Sulfonamides as TRPM8 modulators

ABSTRACT

Disclosed are compounds, compositions and methods for treating various diseases, syndromes, conditions and disorders, including pain. Such compounds are represented by Formula I as follows: 
                         
wherein A, B, G, Y, R 1 , R 2 , R 3 , and R 4  are defined herein.

CROSS REFERENCE TO RELATED APPLICATIONS

This divisional application claims the benefit of parent application Ser. No. 12/175,740, filed 18 Jul. 2008, which is the national stage of Application No. PCT/EP2008/070425, filed 18 Jul. 2008, which application claims priority from PCT/EP08796274.2 filed 18 Jul. 2007.

FIELD OF THE INVENTION

The present invention relates to sulfonamides that act as modulators of the TRPM8 receptor. The present invention also relates to processes for the preparation of sulfonamides and to their use in treating various diseases, syndromes, and disorders, including, those that cause inflammatory or neuropathic pain, cold intolerance or cold allodynia, peripheral vascular pain, itch, urinary incontinence, chronic obstructive pulmonary disease (COPD), pulmonary hypertension and anxiety, including other stress-related disorders, and combinations thereof.

BACKGROUND OF THE INVENTION

Transient receptor potential (TRP) channels are non-selective cation channels that are activated by a variety of stimuli. Numerous members of the ion channel family have been identified to date, including the cold-menthol receptor, also called TRPM8 (McKerny D. D., et al., Nature 2002, 416(6876), 52-58). Collectively, the TRP channels and related TRP-like receptors connote sensory responsivity to the entire continuum of thermal exposure, selectively responding to threshold temperatures ranging from noxious hot through noxious cold as well as to certain chemicals that mimic these sensations. Specifically, TRPM8 is known to be stimulated by cool to cold temperatures as well as by chemical agents such as menthol and icilin, which may be responsible for the therapeutic cooling sensation that these agents provoke. TRPM8 is located on primary nociceptive neurons (A-delta and C-fibers) and is also modulated by inflammation-mediated second messenger signals (Abe, J., et al., Neurosci Lett 2006, 397(1-2), 140-144; Premkumar, L. S., et al., J. Neurosci, 2005, 25(49), 11322-11329). The localization of TRPM8 on both A-delta and C-fibers may provide a basis for abnormal cold sensitivity in pathologic conditions wherein these neurons are altered, resulting in pain, often of a burning nature (Kobayashi, K., et al., J Comp Neurol, 2005, 493(4), 596-606; Roza, C., et al., Pain, 2006, 120(1-2), 24-35; and Xing, H., et al., J Neurophysiol, 2006, 95(2), 1221-30). Cold intolerance and paradoxical burning sensations induced by chemical or thermal cooling closely parallel symptoms seen in a wide range of clinical disorders and thus provide a strong rationale for the development of TRPM8 modulators as novel antihyperalgesic or antiallodynic agents. TRPM8 is also known to be expressed in the brain, lung, bladder, gastrointestinal tract, blood vessels, prostate and immune cells, thereby providing the possibility for therapeutic modulation in a wide range of maladies.

International patent application WO 2006/040136 A1 from Bayer Healthcare AG purportedly describes substituted 4-benzyloxy-phenylmethylamide derivatives as cold menthol receptor-1 (CMR-1) antagonists for the treatment of urological disorders. International patent application WO 2006/040103 A1 from Bayer Healthcare AG purportedly describes methods and pharmaceutical compositions for treatment and/or prophylaxis of respiratory diseases or disorders. International patent applications WO 2007/017092A1, WO 2007/017093A1 and WO 2007/017094A1, from Bayer Healthcare AG, purportedly describe benzyloxyphenylmethyl carbamate, substituted 2-benzyloxybenzoic acid amide and substituted 4-benzyloxybenzoic acid amide derivatives for the treatment of diseases associated with the cold menthol receptor (CMR), a.k.a. TRPM8.

There is a need in the art for TRPM8 antagonists that can be used to treat a disease, syndrome, or condition in a mammal in which the disease, syndrome, or condition is affected by the modulation of TRPM8 receptors, such as pain, the diseases that lead to such pain, and pulmonary or vascular dysfunction.

SUMMARY OF THE INVENTION

The present invention provides, inter alia, compounds of Formula (I)

wherein

A is CR⁵ or N;

B is CR⁶ or N; with the proviso that A and B are C(R⁵) and C(R⁶), respectively, when G is S(O)₂;

G is S or S(O₂);

Y is

-   -   (i) H;     -   (ii) isopropenyl;     -   (iii) C₁₋₆ alkylcarbonyl optionally substituted with 1 chloro or         1 to 3 fluoro substituents;     -   (iv) C₃₋₆ cycloalkylcarbonyl;     -   (v) phenylcarbonyl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl, fluoro, or         chloro;     -   (vi) phenylcarbonyl substituted with trifluoromethyl and         optionally one additional substituent selected from         trifluoromethyl, chloro, fluoro, or C₁₋₄ alkyl;     -   (vii) heteroaryl optionally substituted with one to two         substituents independently selected from chloro, fluoro, bromo,         trifluoromethyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄ alkyl, C₁₋₃         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, amino, C₁₋₃ alkylamino,         or di(C₁₋₃)alkylamino;     -   (viii) benzo-fused heteroaryl optionally substituted with one to         two substituents independently selected from chloro, fluoro,         bromo, trifluoromethyl, C₁₋₄ alkyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, amino, C₁₋₃ alkylamino,         or di(C₁₋₃)alkylamino;     -   (ix) bromo;     -   (x) chloro;     -   (xi) fluoro;     -   (xii) iodo;     -   (xiii) cyano;     -   (xiv) formyl;     -   (xv) C₁₋₆ alkyl optionally substituted with 1 to 3 substituents         independently selected from hydroxy, fluoro, or chloro;     -   (xvi) C(OH)(C₁₋₃ alkyl)₂;     -   (xvii) C₃₋₆ cycloalkyl;     -   (xviii) C₁₋₂ alkyl substituted with 1 substituent independently         selected from C₁₋₄ alkoxycarbonyl, cyano, C₁₋₃ alkylthio, C₁₋₄         alkoxy, or NR⁷R⁸ wherein R⁷ is hydrogen, C₁₋₄ alkyl,         C₁₋₃alkylcarbonyl, or C₁₋₃ alkylsulfonyl and R⁸ is hydrogen or         C₁₋₄ alkyl; or R⁷ and R⁸ are taken together with the nitrogen         atom to which they are attached to form a 5 or 6 membered ring         optionally containing one additional heteroatom selected from         nitrogen, oxygen, or sulfur;     -   (xix) C₁₋₄ alkoxycarbonyl;     -   (xx) C₁₋₃ alkoxy;     -   (xxi) hydroxy;     -   (xxii) C₆₋₁₀ aryl optionally substituted with one to three         substituents independently selected from chloro, fluoro, bromo,         C₁₋₄ alkoxy, hydroxy, C₁₋₃ alkoxycarbonyl, C₁₋₃ alkylthio,         cyano, amino, C₁₋₂ alkylamino, di(C₁₋₂)alkylamino, or C₁₋₆ alkyl         optionally substituted with one to three halogen substituents;         with the proviso that not more than two of the substituents are         selected from the group consisting of C₁₋₃ alkoxycarbonyl, C₁₋₃         alkylthio, cyano, amino, C₁₋₂ alkylamino, di(C₁₋₂)alkylamino,         and C₁₋₆ alkyl substituted with one to three halogen         substituents;     -   (xxiii) NR⁹R¹⁰ wherein R⁹ is hydrogen, C₁₋₄ alkyl,         C₁₋₃alkylcarbonyl, or C₁₋₃ alkylsulfonyl and R¹⁰ is hydrogen or         C₁₋₄ alkyl, or R⁹ and R¹⁰ are taken together with the nitrogen         atom to which they are attached to form a 5 or 6 membered ring         optionally containing one additional heteroatom selected from         nitrogen, oxygen, or sulfur; and wherein said 5 or 6 membered         ring is optionally substituted with a C₁₋₄ alkyl substituent;         with the proviso that when G is S and R¹⁰ is hydrogen, R⁹ is         other than hydrogen and C₁₋₄ alkyl;     -   (xxiv) aminocarbonyl;     -   (xxv) methylaminocarbonyl;     -   (xxvi) dimethylaminocarbonyl; or     -   (xxvii) arylhydroxy(C₁₋₃)alkyl;

R¹ is

-   -   (i) CF₃;     -   (ii) C₁₋₆ alkyl optionally substituted with 1 substituent         selected from C₁₋₃ alkylsulfonyl, C₁₋₄ alkoxycarbonyl, formyl,         hydroxy, carboxy, trifluoromethyl, C₁₋₄ alkoxy, C₁₋₃ alkylthio,         bromo, cyano, R¹¹, or R¹²;     -   (iii) aryl(C₁₋₂ alkyl) wherein the ring of the aryl group is         optionally substituted with 1 to 3 substituents independently         selected from C₁₋₄ alkyl, fluoro, chloro, trifluoromethyl,         hydroxy, C₁₋₄ alkoxy, C₁₋₄ alkoxycarbonyl, or carboxy; with the         proviso that not more than two of the substituents are selected         from the group consisting of trifluoromethyl, C₁₋₄         alkoxycarbonyl, and carboxy;     -   (iv) heteroaryl(C₁₋₆ alkyl) wherein the heteroaryl group is         bound through a nitrogen heteroatom and is selected from         imidazolyl, triazolyl, or tetrazolyl; and wherein the imidazolyl         group is optionally substituted with 1 substituent selected from         C₁₋₄ alkyl, fluoro, chloro, trifluoromethyl, hydroxy, C₁₋₄         alkoxy, C₁₋₄ alkoxycarbonyl, carboxy, aminomethyl,         methylamino-methyl, or dimethylamino-methyl; and imidazolyl is         optionally substituted with one additional substituent selected         from C₁₋₄ alkyl, fluoro, or chloro;     -   (v) C₃₋₈ cycloalkyl or cyclohexyl substituted at the 4-position         with one substitutent selected from the group consisting of         cyano, C₁₋₄ alkoxycarbonyl, carboxy, aminocarbonyl, C₁₋₃         alkylaminocarbonyl, di(C₁₋₃ alkyl)aminocarbonyl, amino-methyl,         methylamino-methyl, dimethylamino-methyl, R¹¹, and R¹²;     -   (vi) benzo-fused C₅₋₆cycloalkyl attached at the benzo portion of         the ring system, and wherein the C₅₋₆cycloalkyl portion of         benzo-fused C₅₋₆cycloalkyl is optionally substituted with amino,         (C₁₋₃alkyl)amino, or di(C₁₋₃alkyl)amino;     -   (vii) phenyl substituted with 3- or 4-imidazolyl, wherein the         point of attachment of the imidazolyl is through a nitrogen         heteroatom; and wherein the imidazolyl is optionally         independently substituted with one to two substituents selected         from the group consisting of C₁₋₃ alkyl, 2-cyano, chloro, bromo,         amino-C₁₋₂ alkyl, (C₁₋₂ alkyl)amino-C₁₋₂ alkyl, and di(C₁₋₂         alkyl)amino-C₁₋₂ alkyl; wherein di(C₁₋₃ alkyl) is optionally         taken together with the nitrogen atom to which it is attached to         form a 5 or 6 membered ring optionally containing one additional         heteroatom selected from nitrogen, oxygen, or sulfur; and         wherein the ring formed by di(C₁₋₃ alkyl)amino is optionally         substituted with C₁₋₃alkyl; with the proviso that not more than         one of the substituents is amino-C₁₋₂ alkyl, (C₁₋₂         alkyl)amino-C₁₋₂ alkyl, or di(C₁₋₂ alkyl)amino-C₁₋₂ alkyl;     -   (viii) phenyl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl optionally         substituted with one to three chloro or fluoro substituents or         one hydroxy substituent, chloro, fluoro, bromo, C₁₋₄ alkoxy,         trifluoromethoxy, 3- or 4-phenyloxy, 3- or 4-heteroaryloxy         wherein the heteroaryl ring is a 6 membered ring containing         carbon ring members and 1 or 2 nitrogen heteroatom ring members,         C₁₋₃ alkylsulfonyl, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio,         hydroxy, carboxy, cyano, nitro, 3- or 4-heteroaryl wherein said         heteroaryl is other than imidazolyl, C₁₋₃ alkylcarbonyl,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃ alkylsulfonylaminocarbonyl,         di(C₁₋₃)alkylaminosulfonyl, P(O)(OC₁₋₃alkyl)₂, P(O)(OH)₂, SO₃H,         C(O)NHOH, C(═N)NH₂, C(═NOH)NH₂, C(═N(methylcarbonyloxy))NH₂, or         SO₂NH₂; with the proviso that not more than two of the         substituents are selected from the group consisting of         trifluoromethoxy, 3- or 4-substituted phenyloxy, 3- or         4-heteroaryloxy, C₁₋₃ alkylsulfonyl, C₁₋₄ alkoxycarbonyl, C₁₋₃         alkylthio, carboxy, cyano, 3- or 4-heteroaryl, C₁₋₃         alkylcarbonyl, aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃ alkylsulfonylaminocarbonyl,         di(C₁₋₃)alkylaminosulfonyl, and P(O)(OC₁₋₃ alkyl)₂ and not more         than one of the substituents is selected from the group         consisting of —P(O)(OH)₂, —SO₃H, carboxy, C(O)NHOH, C(═N)NH₂,         C(═NOH)NH₂, C(═N(C₁₋₃alkylcarbonyloxy))NH₂, and —SO₂NH₂; wherein         the phenyloxy is optionally substituted with one to two         substituents independently selected from the group consisting of         methyl and fluoro;         -   and wherein the heteroaryl substituent is optionally             independently substituted with one to two substituents             selected from the group consisting of C₁₋₃ alkyl,             trifluoromethyl, trifluoromethoxy, cyano, amino,             methylamino, dimethylamino, chloro, bromo, carboxy, C₁₋₂             alkoxycarbonyl, C₁₋₂ alkoxycarbonylmethyl, carboxymethyl,             amino-C₁₋₂ alkyl, (C₁₋₂ alkyl)amino-C₁₋₂ alkyl, and di(C₁₋₂             alkyl)amino-C₁₋₂ alkyl; with the proviso that not more than             one of the substituents is selected from the group             consisting of carboxy, C₁₋₂ alkoxycarbonyl, C₁₋₂             alkoxycarbonylmethyl, carboxymethyl, amino-C₁₋₂ alkyl, (C₁₋₂             alkyl)amino-C₁₋₂ alkyl, and di(C₁₋₂ alkyl)amino-C₁₋₂ alkyl;     -   (ix) naphthyl optionally substituted with one substituent         selected from the group consisting of hydroxy, chloro, fluoro,         bromo, C₁₋₄ alkoxycarbonyl, and carboxy;     -   (x) C₆₋₁₀ aryl substituted with phenyl optionally substituted         with one to two substituents selected from chloro, fluoro, C₁₋₄         alkoxy, C₁₋₄ alkoxycarbonyl, carboxy, hydroxy, or C₁₋₃ alkyl;     -   (xi) phenyl substituted with R¹¹ or R¹² at the 3 or 4 position;         and optionally one additional substituent selected from fluoro,         chloro, or C₁₋₃ alkyl;     -   (xii) pyridin-3-yl substituted at a carbon atom other than that         adjacent to the carbon bearing S(O)₂ with a substituent selected         from N-imidazolyl, oxadiazolyl, thiazolyl, R¹¹, or R¹²; wherein         pyridin-3-yl is optionally substituted with one additional         substituent selected from fluoro, chloro, or C₁₋₃ alkyl; and         further, wherein the N-imidazolyl group is optionally         substituted with one to two substituents, and the oxadiazolyl         and thiazolyl groups are optionally substituted one substituent,         said substituent(s) independently selected from the group         consisting of C₁₋₄ alkyl, trifluoromethyl, cyano, amino,         methylamino, dimethylamino, chloro, bromo, carboxy, C₁₋₂         alkoxycarbonyl, C₁₋₂ alkoxycarbonylmethyl, carboxymethyl,         amino-C₁₋₂ alkyl, (C₁₋₂ alkyl)amino-C₁₋₂ alkyl, and di(C₁₋₂         alkyl)amino-C₁₋₂ alkyl; with the proviso that not more than one         of the substituents is selected from the group consisting of         carboxy, C₁₋₂ alkoxycarbonyl, C₁₋₂ alkoxycarbonylmethyl,         carboxymethyl, trifluoromethyl, cyano, amino-C₁₋₂ alkyl, (C₁₋₂         alkyl)amino-C₁₋₂ alkyl, and di(C₁₋₂ alkyl)amino-C₁₋₂ alkyl;     -   (xiii) imidazolyl substituted with R¹¹ or R¹²; and imidazolyl is         optionally substituted at a nitrogen heteroatom with C₁₋₄ alkyl;     -   (xiv) a ring selected from phenyl or pyridin-3-yl, wherein said         ring is substituted with NR¹⁵R¹⁶; wherein R¹⁵ is hydrogen, C₁₋₄         alkyl, C₁₋₄ alkylcarbonyl, trifluoromethylcarbonyl,         trifluoromethylsulfonyl, C₃₋₆ cycloalkylsulfonyl, or C₁₋₃         alkylsulfonyl; and R¹⁶ is hydrogen or C₁₋₄ alkyl; or R¹⁵ and R¹⁶         are taken together with the nitrogen atom to which they are         attached to form a 5 or 6 membered ring optionally containing         one additional heteroatom selected from nitrogen, oxygen, or         sulfur optionally substituted with one or two oxo substituents;         and wherein the ring formed by NR¹⁵R¹⁶ is optionally substituted         with C₁₋₃alkyl, C₁₋₂ alkoxycarbonyl, or carboxy; and wherein         said phenyl is optionally substituted with one to two additional         substituents independently selected from the group consisting of         C₁₋₄ alkyl, C₁₋₄ alkoxy, hydroxy, fluoro, chloro, and bromo;     -   (xv) phenyl substituted with C(O)NR¹⁷R¹⁸ wherein R¹⁷ is         hydrogen, C₁₋₄ alkyl, C₁₋₄ alkylcarbonyl, pyrrolidin-3-yl, or         C₁₋₃ alkylsulfonyl; and R¹⁸ is hydrogen or C₁₋₄ alkyl; or R¹⁷         and R¹⁸ are taken together with the nitrogen atom to which they         are attached to form a 5 or 6 membered ring optionally         containing one additional heteroatom selected from nitrogen,         oxygen, or sulfur; and wherein said ring is optionally         substituted with C₁₋₃alkyl;     -   (xvi) phenyl substituted with 4 or 5 fluoro substituents;     -   (xvii) phenyl substituted at the 4-position with         -Q-C(R^(x)R^(y))—(CH₂)₀₋₁CO₂H wherein Q is a bond or O; and         wherein R^(x) and R^(y) are independently hydrogen or methyl; or         R^(x) and R^(y) are taken together with the carbon atom to which         they are both attached to form a cyclopropyl ring;     -   (xviii) heteroaryl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl, chloro,         fluoro, bromo, trifluoromethyl, C₁₋₄ alkoxy, oxo, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, carboxy, amino, C₁₋₃         alkylamino, di(C₁₋₃)alkylamino, morpholin-4-yl, or heteroaryl;         wherein the heteroaryl group is optionally independently         substituted with one to two substituents selected from the group         consisting of C₁₋₃ alkyl, trifluoromethyl, fluoro, and chloro;         with the proviso that not more than two of the substituents are         selected from the group consisting of trifluoromethyl, C₁₋₄         alkoxy, oxo, hydroxy, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio,         cyano, carboxy, amino, C₁₋₃ alkylamino, and di(C₁₋₃)alkylamino;     -   (xix) benzo-fused heteroaryl optionally substituted at a carbon         atom with one to three substituents independently selected from         C₁₋₄ alkyl, chloro, fluoro, bromo, difluoromethyl,         trifluoromethyl, C₁₋₄ alkoxy, oxo, hydroxy, C₁₋₄ alkoxycarbonyl,         C₁₋₃ alkylthio, cyano, carboxy, amino, C₁₋₃ alkylamino, or         di(C₁₋₃)alkylamino; with the proviso that not more than two of         the substituents are selected from the group consisting of         trifluoromethyl, C₁₋₄ alkoxy, oxo, hydroxy, C₁₋₄alkoxycarbonyl,         C₁₋₃ alkylthio, cyano, carboxy, amino, C₁₋₃ alkylamino, and         di(C₁₋₃)alkylamino; and benzo-fused heteroaryl is optionally         substituted at a nitrogen atom with C₁₋₃ alkyl;     -   (xx) benzo-fused heterocycle optionally substituted with one to         two substituents independently selected from trifluoromethyl,         C₁₋₃ alkylcarbonyl, C₁₋₄ alkyl, C₁₋₄alkoxy,         trifluoromethylcarbonyl, fluoro, chloro, bromo, hydroxy, oxo,         carboxy, or C₁₋₄ alkoxycarbonyl; such that when the benzo-fused         heterocycle is substituted on the heterocyclic ring, the         substituents on the heterocyclic ring are selected from oxo,         hydroxy, C₁₋₄ alkyl, or trifluoromethylcarbonyl; with the         proviso that not more than one substituent is         trifluoromethylcarbonyl; and with the proviso that when the         benzo-fused heterocycle is substituted with         trifluoromethylcarbonyl, at least one of the ring members of the         heterocycle is a nitrogen heteroatom and the point of attachment         to the trifluoromethylcarbonyl substituent is through the         nitrogen heteroatom;     -   (xxi) amino;     -   (xxii) C₁₋₆ alkylamino; or     -   (xxiii) di(C₁₋₆alkyl)amino;

R² is

-   -   (i) C₃₋₆ cycloalkyl;     -   (ii) C₁₋₂ alkyl substituted with adamantyl or norbornanyl;     -   (iii) C₁₋₆ alkyl substituted with two C₆₋₁₀ aryl groups wherein         one of said aryl groups is optionally substituted with 1 to 3         substituents independently selected from chloro, fluoro, bromo,         C₁₋₄ alkyl, C₁₋₄ alkoxy optionally substituted with 1 to 3         fluoro substituents, hydroxy, C₁₋₄alkoxycarbonyl, C₁₋₃         alkylthio, cyano, trifluoromethyl, aminocarbonyl, C₁₋₃         alkylaminocarbonyl, di(C₁₋₃)alkylaminocarbonyl, C₁₋₃         alkylsulfonyl optionally substituted with 1 to 3 fluoro         substituents, nitro, amino, C₁₋₃ alkylamino, di(C₁₋₃)alkylamino,         or C₁₋₃alkylcarbonyl; with the proviso that not more than two of         the substituents are selected from the group consisting of C₁₋₄         alkoxy substituted with 1 to 3 fluoro substituents, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, trifluoromethyl,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃ alkylsulfonyl optionally         substituted with 1 to 3 fluoro substituents, nitro, amino, C₁₋₃         alkylamino, di(C₁₋₃)alkylamino, and C₁₋₃alkylcarbonyl; and the         other of said aryl groups is optionally substituted with 1         substituent selected from chloro, fluoro, bromo, C₁₋₄ alkyl,         C₁₋₄ alkoxy optionally substituted with 1 to 3 fluoro         substituents, hydroxy, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio,         cyano, trifluoromethyl, aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃ alkylsulfonyl optionally         substituted with 1 to 3 fluoro substituents, nitro, amino, C₁₋₃         alkylamino, di(C₁₋₃)alkylamino, or C₁₋₃alkylcarbonyl;     -   (iv) C₁₋₆ alkyl substituted with one C₆₋₁₀ aryl group and         optionally one additional substituent selected from hydroxy or         oxo, wherein said C₆₋₁₀ aryl group is optionally substituted         with 1 to 3 substituents independently selected from chloro,         fluoro, bromo, C₁₋₄ alkyl, C₁₋₄ alkoxy optionally substituted         with 1 to 3 fluoro substituents, hydroxy, C₁₋₄ alkoxycarbonyl,         C₁₋₃ alkylthio, trifluoromethylthio, cyano, trifluoromethyl,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃ alkylsulfonyl optionally         substituted with 1 to 3 fluoro substituents, nitro, amino, C₁₋₃         alkylamino, di(C₁₋₃)alkylamino, or C₁₋₃alkylcarbonyl; with the         proviso that not more than two of the substituents are selected         from the group consisting of C₁₋₄ alkoxy substituted with 1 to 3         fluoro substituents, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio,         trifluoromethylthio, cyano, trifluoromethyl, aminocarbonyl, C₁₋₃         alkylaminocarbonyl, di(C₁₋₃)alkylaminocarbonyl, C₁₋₃         alkylsulfonyl optionally substituted with 1 to 3 fluoro         substituents, nitro, amino, C₁₋₃ alkylamino, di(C₁₋₃)alkylamino,         and C₁₋₃ alkylcarbonyl;     -   (v) C₁₋₆ alkyl substituted with phenyl, wherein phenyl is         substituted with 4 or 5 fluoro substituents; or phenyl is         substituted with methoxy and 3 to 4 fluoro substituents;     -   (vi) C₁₋₆ alkyl substituted with one heteroaryl group and         optionally one additional substituent selected from oxo or         hydroxy wherein said heteroaryl group is optionally substituted         with one to three fluoro substituents or 1 substituent selected         from chloro, bromo, trifluoromethyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, or C₁₋₄ alkyl;     -   (vii) C₁₋₆ alkyl substituted with one benzo-fused heteroaryl         group and optionally one additional substituent selected from         oxo or hydroxy, wherein said benzo-fused heteroaryl group is         optionally substituted with 1 substituent selected from chloro,         fluoro, bromo, trifluoromethyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, or C₁₋₄ alkyl;     -   (viii) C₁₋₆ alkyl substituted with one heterocycle group wherein         said heterocycle group is optionally substituted with one to         three substituents independently selected from C₁₋₄ alkyl, C₁₋₄         alkoxycarbonyl, oxo, or hydroxy; with the proviso that not more         than two of the substituents are selected from the group         consisting of oxo and hydroxy;     -   (ix) C₁₋₆ alkyl substituted with benzo[1,3]dioxol-5-yl,         2,2-difluoro-benzo[1,3]dioxol-5-yl, or         2,3-dihydro-benzo[1,4]dioxin-6-yl; or     -   (x) C₂₋₆ alkyl optionally substituted with 1 to 2 substituents         independently selected from cyano, trifluoromethyl, C₁₋₆         alkylcarbonyl, C₁₋₆ alkylthio, C₁₋₆ alkylsulfonyl, amino, C₁₋₃         alkylamino, di(C₁₋₃)alkylamino, C₂₋₆ alkenyl, C₂₋₆ alkynyl,         fluoro, C₁₋₆ alkoxy, C₁₋₆ alkoxycarbonyl, C₁₋₄         alkoxycarbonylamino, hydroxy, P(O)(OC₁₋₃)₂, C₃₋₆ cycloalkyloxy,         C₃₋₄ cycloalkyl, or C₅₋₈ cycloalkyl optionally substituted with         one to three substituents independently selected from the group         consisting of halogen, hydroxy, oxo and C₁₋₄ alkyl optionally         substituted with one to three substituents independently         selected from halogen or hydroxy; with the proviso that not more         than one of the substituents on the C₁₋₄ alkyl of the C₁₋₄ alkyl         substituted C₅₋₈ cycloalkyl is hydroxy, and not more than two of         the substituents on the C₅₋₈ cycloalkyl are oxo;

R³ is

-   -   (i) hydrogen,     -   (ii) C₁₋₆ alkyl,     -   (iii) trifluoromethyl,     -   (iv) C₁₋₄ alkoxy,     -   (v) bromo,     -   (vi) chloro,     -   (vii) fluoro, or     -   (viii) hydroxy;

R⁴ is

-   -   (i) hydrogen,     -   (ii) fluoro,     -   (iii) chloro, or     -   (iv) methyl;

R⁵ is hydrogen;

R⁶ is

-   -   (i) hydrogen,     -   (ii) fluoro,     -   (iii) chloro,     -   (iv) methoxy, or     -   (v) methyl;

R¹¹ is selected from

R¹² is selected from

wherein R¹³ is H, —C₁₋₄ alkyl, —CH₂CO₂CH₃, —CH₂NH(C₁₋₃alkyl), —CH₂N(C₁₋₃alkyl)₂, or —CH₂CO₂H; and R¹⁴ is —C₆₋₁₀ aryl, —C₁₋₆ alkyl, —C₁₋₃ alkyl-OH, or —C₁₋₃alkylCO₂H;

with the proviso that when R¹ is C₆₋₁₀ aryl, wherein C₆₋₁₀ aryl is phenyl, substituted with carboxy at the 2 position, Y is not hydrogen;

with the proviso that when R² is C₁₋₆ alkyl substituted with at least one P(O)(OCH₃)₂ substituent, R¹ is optionally substituted C₆₋₁₀ aryl;

with the proviso that when R² is C₁₋₆ alkyl substituted with at least one C₁₋₆ alkoxycarbonyl substituent, R¹ is optionally substituted C₆₋₁₀ aryl;

with the proviso that when Y is unsubstituted phenyl, and R¹ is ethyl, R² is not 4-fluoro-3-trifluoromethyphenylmethyl;

with the proviso that when R² is C₁₋₆ alkyl substituted with an unsubstituted heterocycle comprising at least one nitrogen heteroatom, the point of attachment to the pendant group is through a nitrogen heteroatom;

with the proviso that when R² is substituted or unsubstituted C₁₋₆ alkyl, R¹ is other than phenyl substituted at the 3-position with R¹¹ or R¹²;

with the proviso that Formula (I) is other than

-   a compound wherein G is S, Y is H, R¹ is 4-cyanophenyl, R² is     4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and     B is CR⁶; -   a compound wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is     octahydro-quinolizin-1-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A     is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is 1-hydroxyethyl, R¹ is     2,2,2-trifluoroethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl,     R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is methyl, R¹ is     4-piperazin-1-ylcarbonylphenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴,     R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is methylcarbonylamino, R¹ is     4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A     is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is H, R¹ is 3-aminocarbonylphenyl, R²     is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are     hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is bromo, R¹ is     4-(1-hydroxy-1-methyl-ethyl)phenyl, R² is     4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are     hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is methylaminocarbonyl, R¹ is     4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A     is CR⁵, and B is CR⁶; -   a compound wherein G is S(O₂), Y is methyl, R¹ is 4-carboxyphenyl,     R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is     CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is H, R¹ is     4-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is n-butyl,     R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is 4-methyl-piperazin-1-ylcarbonyl, R¹     is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵,     and R⁶ are hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is bromo, R¹ is     4-(1-hydroxyethyl)phenyl, R² is     4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are     hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is dimethylaminomethyl, R¹ is     4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A     is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is H, R¹ is 3-cyanophenyl, R² is     5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵,     and B is CR⁶; -   a compound wherein G is S, Y is methylcarbonyl, R¹ is     4-carboxyphenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are     hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is H, R¹ is 4-carboxyphenyl, R² is     2-fluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is     CR⁶; -   a compound wherein G is S, Y is H, R¹ is 4-carboxyphenyl, R² is     3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is     CR⁶; and -   a compound wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is     2-fluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is     CR⁶; -   a compound wherein G is S(O₂), Y is methyl, R¹ is 4-carboxyphenyl,     R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is     CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is H, R¹ is 3-(1H-tetrazol-5-yl)phenyl,     R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are     hydrogen, A is CR⁵, and B is CR⁶;

and enantiomers, diastereomers, solvates, and pharmaceutically acceptable salts thereof.

The present invention also provides, inter alia, a pharmaceutical composition comprising, consisting of and/or consisting essentially of a pharmaceutically acceptable carrier, a pharmaceutically acceptable excipient, and/or a pharmaceutically acceptable diluent and a compound of Formula (I) or a pharmaceutically acceptable salt form thereof.

Also provided are processes for making a pharmaceutical composition comprising, consisting of, and/or consisting essentially of admixing a compound of Formula (I) and a pharmaceutically acceptable carrier, a pharmaceutically acceptable excipient, and/or a pharmaceutically acceptable diluent.

The present invention further provides, inter alia, methods for treating or ameliorating a TRPM8-modulated disorder in a subject, including a mammal and/or human in which the disease, syndrome, or condition is affected by the modulation of TRPM8 receptors, such as pain, the diseases that lead to such pain, and pulmonary or vascular dysfunction using a compound of Formula (I). In particular, the methods of the present invention are directed to treating or ameliorating a TRPM8 receptor-modulated disorder including inflammatory pain, cold-intolerance or cold allodynia, peripheral vascular pain, itch, urinary incontinence, chronic obstructive pulmonary disease, pulmonary hypertension and anxiety, including other stress-related disorders, using a compound of Formula (I).

The present invention also provides, inter alia, methods for producing the instant compounds and pharmaceutical compositions and medicaments thereof. A process included in the scope of this invention includes the following process for the preparation of Compound 306

Comprising, consisting of and/or consisting essentially of

reacting a compound of formula X with t-butyl alcohol and a tertiary amine; in an organic solvent; followed by the addition of a mixture of diphenylphosphorylazide in an organic solvent; at temperature of about 110° C.; to yield a compound of formula XI;

reacting a compound of formula XI with a mineral acid or organic acid; neat or in an organic solvent; at temperature of from about 21° C. to about 22° C.; to yield a compound of formula XII;

reacting a compound of formula XII with 4-(chlorosulfonyl)benzoic acid; in an organic solvent; at a temperature of about 21° C. to about 22° C.; to afford a compound of Formula XIII;

reacting a compound of Formula XIII in the presence of methanol; followed by the addition of sulfuric acid; at a temperature of from about 64° C. to about 65° C.; to afford a compound of the Formula XIV;

reacting a compound of Formula XIV in an organic solvent; in the presence of an inorganic base; followed by the addition of 4-fluoro-3-(trifluoromethyl)benzyl bromide; at a temperature of from about 21° C. to about 22° C.; to afford Compound 141;

treating Compound 141 with a metal hydroxide; neat or in an organic solvent; at a temperature of about 64° C. to about 66° C.; to afford Compound 306.

DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

The present invention provides, inter alia, compounds of Formula (I)

wherein

A is CR⁵ or N;

B is CR⁶ or N;

Y is

-   -   (i) H;     -   (ii) C₁₋₆ alkylcarbonyl optionally substituted with 1 chloro         substituent or 1 to 3 fluoro substituents;     -   (iii) C₃₋₆ cycloalkylcarbonyl;     -   (iv) phenylcarbonyl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl, fluoro, or         chloro;     -   (v) phenylcarbonyl substituted with trifluoromethyl and         optionally one additional substituent selected from         trifluoromethyl, chloro, fluoro, or C₁₋₄ alkyl;     -   (vi) heteroaryl optionally substituted with one to two         substituents independently selected from chloro, fluoro, bromo,         trifluoromethyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄ alkyl, C₁₋₃         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, amino, C₁₋₃ alkylamino,         or di(C₁₋₃)alkylamino;     -   (vii) benzo-fused heteroaryl optionally substituted with one to         two substituents independently selected from chloro, fluoro,         bromo, trifluoromethyl, C₁₋₄ alkyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, amino, C₁₋₃ alkylamino,         or di(C₁₋₃)alkylamino;     -   (viii) bromo;     -   (ix) chloro;     -   (x) fluoro;     -   (xi) iodo;     -   (xii) cyano;     -   (xiii) formyl;     -   (xiv) C₁₋₆ alkyl optionally substituted with 1 to 3 substituents         independently selected from hydroxy, fluoro, or chloro;     -   (xv) C(OH)(C₁₋₃ alkyl)₂;     -   (xvi) C₃₋₆ cycloalkyl;     -   (xvii) C₁₋₆ alkyl substituted with 1 substituent independently         selected from C₁₋₄ alkoxycarbonyl, cyano, C₁₋₃ alkylthio, C₁₋₄         alkoxy, or NR⁷R⁸ wherein R⁷ is hydrogen, C₁₋₄ alkyl,         C₁₋₃alkylcarbonyl, or C₁₋₃ alkylsulfonyl and R⁸ is hydrogen or         C₁₋₄ alkyl; or R⁷ and R⁸ are taken together with the nitrogen         atom to which they are attached to form a 5 or 6 membered ring         optionally containing one additional heteroatom selected from         nitrogen, oxygen, or sulfur;     -   (xviii) C₁₋₄ alkoxycarbonyl;     -   (xix) C₁₋₃ alkoxy;     -   (xx) hydroxy;     -   (xxi) C₆₋₁₀ aryl optionally with one to three substituents         independently selected from chloro, fluoro, bromo, C₁₋₄ alkoxy,         hydroxy, C₁₋₃ alkoxycarbonyl, C₁₋₃ alkylthio, cyano, amino, C₁₋₂         alkylamino, di(C₁₋₂)alkylamino, or C₁₋₆ alkyl optionally         substituted with one to three halogen substituents; with the         proviso that not more than two of the substituents are selected         from the group consisting of C₁₋₃ alkoxycarbonyl, C₁₋₃         alkylthio, cyano, amino, C₁₋₂ alkylamino, di(C₁₋₂)alkylamino,         and C₁₋₆ alkyl substituted with one to three halogen         substituents;     -   (xxii) NR⁹R¹⁰ wherein R⁹ is hydrogen, C₁₋₄ alkyl,         C₁₋₃alkylcarbonyl, or C₁₋₃ alkylsulfonyl and R¹⁰ is hydrogen or         C₁₋₄ alkyl, or R⁹ and R¹⁰ are taken together with the nitrogen         atom to which they are attached to form a 5 or 6 membered ring         optionally containing one additional heteroatom selected from         nitrogen, oxygen, or sulfur; or     -   (xxiii) arylhydroxy(C₁₋₃)alkyl;

R¹ is

-   -   (i) C₁₋₆ alkyl optionally substituted with 1 substituent         selected from C₁₋₃ alkylsulfonyl, C₁₋₄ alkoxycarbonyl, hydroxy,         carboxy, trifluoromethyl, C₁₋₄ alkoxy, C₁₋₃ alkylthio, or cyano;     -   (ii) aryl(C₁₋₂alkyl) wherein the ring of the aryl group is         optionally substituted with 1 to 3 substituents independently         selected from C₁₋₄ alkyl, fluoro, chloro, trifluoromethyl,         hydroxy, C₁₋₄ alkoxy, C₁₋₄ alkoxycarbonyl, or carboxy; with the         proviso that not more than two of the substituents are selected         from the group consisting of trifluoromethyl, C₁₋₄         alkoxycarbonyl, and carboxy;     -   (iii) heteroaryl(C₁₋₂ alkyl) wherein the ring of the heteroaryl         group is optionally substituted with 1 to 2 substituents         independently selected from C₁₋₄ alkyl, fluoro, chloro,         trifluoromethyl, hydroxy, C₁₋₄ alkoxy, C₁₋₄ alkoxycarbonyl, or         carboxy;     -   (iv) C₃₋₈ cycloalkyl;     -   (v) C₆₋₁₀ aryl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl optionally         substituted with one to three chloro or fluoro substituents,         chloro, fluoro, bromo, C₁₋₄ alkoxy, phenyloxy, heteroaryloxy         wherein the heteroaryl ring is a 6 membered ring containing         carbon ring members and 1 or 2 nitrogen heteroatom ring members,         C₁₋₃ alkylsulfonyl, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio,         hydroxy, carboxy, cyano, heteroaryl, C₁₋₃ alkylcarbonyl,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, P(O)(OC₁₋₃ alkyl)₂, P(O)(OH)₂, SO₃H,         C(O)NHOH, or SO₂NH₂; with the proviso that not more than two of         the substituents are selected from the group consisting of         phenyloxy, heteroaryloxy, C₁₋₃ alkylsulfonyl, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, carboxy, cyano, heteroaryl, C₁₋₃         alkylcarbonyl, aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, and P(O)(OC₁₋₃ alkyl)₂ and not more         than one of the substituents is selected from the group         consisting of —P(O)(OH)₂, —SO₃H, carboxy, C(O)NHOH, and —SO₂NH₂;     -   (vi) C₆₋₁₀ aryl substituted with phenyl optionally substituted         with one to two substituents selected from chloro, fluoro, C₁₋₄         alkoxy, C₁₋₄ alkoxycarbonyl, carboxy, hydroxy, or C₁₋₃ alkyl;     -   (vii) phenyl substituted with R¹¹ or R¹² at the 3 or 4 position;         and optionally one additional substituent selected from fluoro,         chloro, or C₁₋₃ alkyl;     -   (viii) phenyl substituted with 4 or 5 fluoro substituents;     -   (ix) heteroaryl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl, chloro,         fluoro, bromo, trifluoromethyl, C₁₋₄ alkoxy, oxo, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, carboxy, amino, C₁₋₃         alkylamino, or di(C₁₋₃)alkylamino; with the proviso that not         more than two of the substituents are selected from the group         consisting of trifluoromethyl, C₁₋₄ alkoxy, oxo, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, carboxy, amino, C₁₋₃         alkylamino, and di(C₁₋₃)alkylamino;     -   (x) benzo-fused heteroaryl optionally substituted with one to         three substituents independently selected from C₁₋₄ alkyl,         chloro, fluoro, bromo, trifluoromethyl, C₁₋₄ alkoxy, oxo,         hydroxy, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio, cyano, carboxy,         amino, C₁₋₃ alkylamino, or di(C₁₋₃)alkylamino; with the proviso         that not more than two of the substituents are selected from the         group consisting of trifluoromethyl, C₁₋₄ alkoxy, oxo, hydroxy,         C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio, cyano, carboxy, amino, C₁₋₃         alkylamino, and di(C₁₋₃)alkylamino;     -   (xi) benzo-fused heterocycle optionally substituted with one to         two substituents independently selected from trifluoromethyl,         C₁₋₃ alkylcarbonyl, C₁₋₄ alkyl, C₁₋₄ alkoxy,         trifluoromethylcarbonyl, fluoro, chloro, bromo, hydroxy, oxo,         carboxy, or C₁₋₄ alkoxycarbonyl; such that when the benzo-fused         heterocycle is substituted on the heterocyclic ring, the         substituents on the heterocyclic ring are selected from oxo,         hydroxy, C₁₋₄ alkyl, or trifluoromethylcarbonyl; with the         proviso that not more than one substituent is         trifluoromethylcarbonyl; and with the proviso that when the         benzo-fused heterocycle is substituted with         trifluoromethylcarbonyl, at least one of the ring members of the         heterocycle is a nitrogen heteroatom and the point of attachment         to the trifluoromethylcarbonyl substituent is through the         nitrogen heteroatom;     -   (xii) amino;     -   (xiii) C₁₋₆ alkylamino; or     -   (xiv) di(C₁₋₆alkyl)amino;

R² is

-   -   (i) C₃₋₆ cycloalkyl;     -   (ii) C₁₋₂ alkyl substituted with adamantyl;     -   (iii) C₁₋₆ alkyl substituted with two C₆₋₁₀ aryl groups wherein         one of said aryl groups is optionally substituted with 1 to 3         substituents independently selected from chloro, fluoro, bromo,         C₁₋₄ alkyl, C₁₋₄ alkoxy optionally substituted with 1 to 3         fluoro substituents, hydroxy, C₁₋₄ alkoxycarbonyl,         C₁₋₃alkylthio, cyano, trifluoromethyl, aminocarbonyl, C₁₋₃         alkylaminocarbonyl, di(C₁₋₃)alkylaminocarbonyl,         C₁₋₃alkylsulfonyl optionally substituted with 1 to 3 fluoro         substituents, nitro, amino, C₁₋₃alkylamino, di(C₁₋₃)alkylamino,         or C₁₋₃alkylcarbonyl; with the proviso that not more than two of         the substituents are selected from the group consisting of C₁₋₄         alkoxy substituted with 1 to 3 fluoro substituents, C₁₋₄         alkoxycarbonyl, C₁₋₃alkylthio, cyano, trifluoromethyl,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃alkylsulfonyl optionally         substituted with 1 to 3 fluoro substituents, nitro, amino,         C₁₋₃alkylamino, di(C₁₋₃)alkylamino, and C₁₋₃alkylcarbonyl; and         the other of said aryl groups is optionally substituted with 1         substituent selected from chloro, fluoro, bromo, C₁₋₄ alkyl,         C₁₋₄ alkoxy optionally substituted with 1 to 3 fluoro         substituents, hydroxy, C₁₋₄ alkoxycarbonyl, C₁₋₃alkylthio,         cyano, trifluoromethyl, aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃alkylsulfonyl optionally         substituted with 1 to 3 fluoro substituents, nitro, amino, C₁₋₃         alkylamino, di(C₁₋₃)alkylamino, or C₁₋₃alkylcarbonyl;     -   (iv) C₁₋₆ alkyl substituted with one C₆₋₁₀ aryl group and         optionally one additional substituent selected from hydroxy or         oxo, wherein said C₆₋₁₀ aryl group is optionally substituted         with 1 to 3 substituents independently selected from chloro,         fluoro, bromo, C₁₋₄ alkyl, C₁₋₄ alkoxy optionally substituted         with 1 to 3 fluoro substituents, hydroxy, C₁₋₄ alkoxycarbonyl,         C₁₋₃alkylthio, cyano, trifluoromethyl, aminocarbonyl, C₁₋₃         alkylaminocarbonyl, di(C₁₋₃)alkylaminocarbonyl,         C₁₋₃alkylsulfonyl optionally substituted with 1 to 3 fluoro         substituents, nitro, amino, C₁₋₃alkylamino, di(C₁₋₃)alkylamino,         or C₁₋₃alkylcarbonyl; with the proviso that not more than two of         the substituents are selected from the group consisting of C₁₋₄         alkoxy substituted with 1 to 3 fluoro substituents, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, trifluoromethyl,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃ alkylsulfonyl optionally         substituted with 1 to 3 fluoro substituents, nitro, amino, C₁₋₃         alkylamino, di(C₁₋₃)alkylamino, and C₁₋₃ alkylcarbonyl;     -   (v) C₁₋₆ alkyl substituted with one heteroaryl group and         optionally one additional substituent selected from oxo or         hydroxy wherein said heteroaryl group is optionally substituted         with 1 substituent selected from chloro, fluoro, bromo,         trifluoromethyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄ alkoxycarbonyl, C₁₋₃         alkylthio, cyano, or C₁₋₄ alkyl;     -   (vi) C₁₋₆ alkyl substituted with one benzo-fused heteroaryl         group and optionally one additional substituent selected from         oxo or hydroxy, wherein said benzo-fused heteroaryl group is         optionally substituted with 1 substituent selected from chloro,         fluoro, bromo, trifluoromethyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, or C₁₋₄ alkyl;     -   (vii) C₁₋₆ alkyl substituted with one heterocycle group wherein         said heterocycle group is optionally substituted with one to         three substituents independently selected from C₁₋₄ alkyl, C₁₋₄         alkoxycarbonyl, oxo, or hydroxy; with the proviso that not more         than two of the substituents are selected from the group         consisting of oxo and hydroxy; or     -   (viii) C₁₋₆ alkyl optionally substituted with 1 to 2         substituents independently selected from cyano, trifluoromethyl,         C₁₋₆ alkylcarbonyl, C₁₋₆alkylthio, C₁₋₆alkylsulfonyl, amino,         C₁₋₃ alkylamino, di(C₁₋₃)alkylamino, C₂₋₆ alkenyl, C₂₋₆ alkynyl,         fluoro, C₁₋₆ alkoxy, C₁₋₆ alkoxycarbonyl,         C₁₋₄alkoxycarbonylamino, hydroxy, P(O)(OC₁₋₃)₂, C₃₋₄ cycloalkyl,         or C₅₋₈ cycloalkyl optionally substituted with one to three         substituents independently selected from the group consisting of         halogen, hydroxy, oxo and C₁₋₄ alkyl optionally substituted with         one to three substituents independently selected from halogen or         hydroxy; with the proviso that not more than one of the         substituents on the C₁₋₄ alkyl of the C₁₋₄ alkyl substituted         C₅₋₈ cycloalkyl is hydroxy, and not more than two of the         substituents on the C₅₋₈ cycloalkyl are oxo;

R³ is

-   -   (i) hydrogen,     -   (ii) C₁₋₆ alkyl,     -   (iii) trifluoromethyl,     -   (ix) C₁₋₄ alkoxy,     -   (x) bromo,     -   (xi) chloro,     -   (xii) fluoro, or     -   (xiii) hydroxy;

R⁴ is

-   -   (i) hydrogen,     -   (ii) fluoro,     -   (iii) chloro, or     -   (iv) methyl;

R⁵ is hydrogen;

R⁶ is

-   -   (i) hydrogen,     -   (ii) fluoro,     -   (iii) chloro,     -   (iv) methoxy, or     -   (v) methyl;

R¹¹ is selected from

R¹² is selected from

wherein R¹³ is H, —C₁₋₄ alkyl, —CH₂CO₂CH₃, or —CH₂CO₂H; and R¹⁴ is —C₆₋₁₀ aryl, —C₁₋₆ alkyl, —C₁₋₃ alkyl-OH, or —C₁₋₃alkylCO₂H;

with the proviso that when R¹ is C₆₋₁₀ aryl, wherein C₆₋₁₀ aryl is phenyl, substituted with carboxy at the 2 position, Y is not hydrogen;

with the proviso that when R² is C₁₋₆ alkyl substituted with at least one P(O)(OCH₃)₂ substituent, R¹ is optionally substituted C₆₋₁₀ aryl;

with the proviso that when R² is C₁₋₆ alkyl substituted with at least one C₁₋₆ alkoxycarbonyl substituent, R¹ is optionally substituted C₆₋₁₀ aryl;

with the proviso that when Y is unsubstituted phenyl, and R¹ is ethyl, R² is not 4-fluoro-3-trifluoromethyphenylmethyl;

with the proviso that when R² is C₁₋₆ alkyl substituted with an unsubstituted heterocycle comprising at least one nitrogen heteroatom, the point of attachment to the pendant group is through a nitrogen heteroatom;

and enantiomers, diastereomers, racemates, and pharmaceutically acceptable salts thereof.

As used herein, with reference to substituents, the term “independently” means that when more than substituent is possible, the substituents may be the same or different from each other.

As used herein, unless otherwise noted, the term “alkyl” whether used alone or as part of a substituent group, refers to straight and branched carbon chains having 1 to 8 carbon atoms. Therefore, designated numbers of carbon atoms (e.g. C₁₋₈) refer independently to the number of carbon atoms in an alkyl moiety or to the alkyl portion of a larger alkyl-containing substituent. In substituent groups with multiple alkyl groups such as (C₁₋₆alkyl)₂amino- the C₁₋₆alkyl groups of the dialkylamino may be the same or different.

As used herein, unless otherwise noted, the term “alkoxy” refers to an —O-alkyl group, wherein the term “alkyl” is as defined above.

As used herein, unless otherwise noted, the terms “alkenyl” and “alkynyl” refer to straight and branched carbon chains having 2 or more carbon atoms, wherein an alkenyl chain contains at least one double bond and an alkynyl chain contains at least one triple bond.

As used herein, unless otherwise noted, the term “cycloalkyl” refers to saturated or partially saturated, monocyclic or polycyclic hydrocarbon rings of 3 to 14 carbon atoms. Examples of such rings include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and adamantyl.

As used herein, unless otherwise noted, the term “heterocycle” refers to a nonaromatic monocyclic or bicyclic ring system having 3 to 10 ring members and which contains carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, O, and S. Included within the term heterocycle is a nonaromatic cyclic ring of 5 to 7 members in which 1 to 2 members are nitrogen, or a nonaromatic cyclic ring of 5 to 7 members in which zero, one or two members are nitrogen and up to two members are oxygen or sulfur and at least one member must be either nitrogen, oxygen or sulfur; wherein, optionally, the ring contains zero to one unsaturated bonds, and, optionally, when the ring is of 6 or 7 members, it contains up to two unsaturated bonds. The carbon atom ring members that form a heterocycle ring may be fully saturated or partially saturated. The term “heterocycle” also includes two 5 membered monocyclic heterocycloalkyl groups bridged to form a bicyclic ring. Such groups are not considered to be fully aromatic and are not referred to as heteroaryl groups. When a heterocycle is bicyclic, both rings of the heterocycle are non-aromatic and at least one of the rings contains a heteroatom ring member. Examples of heterocycle groups include, and are not limited to, pyrrolinyl (including 2H-pyrrole, 2-pyrrolinyl or 3-pyrrolinyl), pyrrolidinyl, imidazolinyl, imidazolidinyl, pyrazolinyl, pyrazolidinyl, piperidinyl, morpholinyl, thiomorpholinyl, and piperazinyl. Unless otherwise noted, the heterocycle is attached to its pendant group at any heteroatom or carbon atom that results in a stable structure.

As used herein, unless otherwise noted, the term “benzo-fused heterocycle” refers to a 5 to 7 membered monocyclic heterocycle ring fused to a benzene ring. The heterocycle ring contains carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, O, and S. The carbon atom ring members that form the heterocycle ring may be fully saturated or partially saturated. The benzo-fused heterocycle ring is attached to its pendant group at a carbon atom of the benzene ring.

As used herein, unless otherwise noted, the term “aryl” refers to an unsaturated, aromatic monocyclic or bicyclic ring of 6 to 10 carbon members. Examples of aryl rings include phenyl and naphthalenyl.

As used herein, unless otherwise noted, the term “heteroaryl” refers to an aromatic monocyclic or bicyclic aromatic ring system having 5 to 10 ring members and which contains carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, O, and S. Included within the term heteroaryl are aromatic rings of 5 or 6 members wherein the ring consists of carbon atoms and has at least one heteroatom member. Suitable heteroatoms include nitrogen, oxygen, and sulfur. In the case of 5 membered rings, the heteroaryl ring preferably contains one member of nitrogen, oxygen or sulfur and, in addition, up to three additional nitrogens. In the case of 6 membered rings, the heteroaryl ring preferably contains from one to three nitrogen atoms. For the case wherein the 6 membered ring has three nitrogens, at most two nitrogen atoms are adjacent. When a heteroaryl is bicyclic, at least one heteroatom is present in each ring. Examples of heteroaryl groups include furyl, thienyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, triazolyl, thiadiazolyl, pyridinyl, pyridazinyl, pyrimidinyl and pyrazinyl. Unless otherwise noted, the heteroaryl is attached to its pendant group at any heteroatom or carbon atom that results in a stable structure.

As used herein, unless otherwise noted, the term “benzo fused heteroaryl” refers to a 5 to 6 membered monocyclic heteroaryl ring fused to a benzene ring. The heteroaryl ring contains carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, O, and S. Examples of heteroaryl groups with the optionally fused benzene rings include indolyl, isoindolyl, indolinyl, benzofuryl, benzothienyl, indazolyl, benzimidazolyl, benzthiazolyl, benzoxazolyl, benzisoxazolyl, benzothiadiazolyl, benzotriazolyl, quinolinyl, isoquinolinyl and quinazolinyl. Unless otherwise noted, the benzo-fused heteroaryl is attached to its pendant group at any heteroatom or carbon atom that results in a stable structure.

The term “halogen” or “halo” refers to fluorine, chlorine, bromine and iodine.

The term “formyl” refers to the group —C(═O)H.

As used herein, unless otherwise noted, the term “alkylsulfonyl,” refers to the group —S(O)₂—R′ where R′ is an alkyl group as previously defined.

As used herein, unless otherwise noted, the term “alkylsulfanyl,” refers to the group —SR′ where R′ is an alkyl group as previously defined.

The term “oxo” refers to the group (═O).

Whenever the term “alkyl” or “aryl” or either of their prefix roots appear in a name of a substituent (e.g., arylalkyl, alkylamino) the name is to be interpreted as including those limitations given above for “alkyl” and “aryl.” Designated numbers of carbon atoms (e.g., C₁-C₆) refer independently to the number of carbon atoms in an alkyl moiety, an aryl moiety, or in the alkyl portion of a larger substituent in which alkyl appears as its prefix root. For alkyl and alkoxy substituents, the designated number of carbon atoms includes all of the independent members included within a given range specified. For example C₁₋₆ alkyl would include methyl, ethyl, propyl, butyl, pentyl and hexyl individually as well as sub-combinations thereof (e.g. C₁₋₂, C₁₋₃, C₁₋₄, C₁₋₅, C₂₋₆, C₃₋₆, C₄₋₆, C₅₋₆, C₂₋₅, etc.).

In general, under standard nomenclature rules used throughout this disclosure, the terminal portion of the designated side chain is described first followed by the adjacent functionality toward the point of attachment. Thus, for example, a “C₁-C₆ alkylcarbonyl” substituent refers to a group of the formula:

As used herein, the term “R” at a stereocenter designates that the stereocenter is purely of the R-configuration as defined in the art; likewise, the term “S” means that the stereocenter is purely of the S-configuration. As used herein, the terms “*R” or “*S” at a stereocenter are used to designate that the stereocenter is of pure but unknown configuration. As used herein, the term “RS” refers to a stereocenter that exists as a mixture of the R- and S-configurations. Similarly, the terms “*RS” or “*SR” refer to a stereocenter that exists as a mixture of the R- and S-configurations and is of unknown configuration relative to another stereocenter within the molecule.

Compounds containing one stereocenter drawn without a stereo bond designation are a mixture of two enantiomers. Compounds containing two stereocenters both drawn without stereo bond designations are a mixture of four diastereomers. Compounds with two stereocenters both labeled “RS” and drawn with stereo bond designations are a two-component mixture with relative stereochemistry as drawn. Compounds with two stereocenters both labeled “*RS” and drawn with stereo bond designations are a two-component mixture with relative stereochemistry unknown. Unlabeled stereocenters drawn without stereo bond designations are a mixture of the R- and S-configurations. For unlabeled stereocenters drawn with stereo bond designations, the absolute stereochemistry is as depicted.

Unless otherwise noted, it is intended that the definition of any substituent or variable at a particular location in a molecule be independent of its definitions elsewhere in that molecule. It is understood that substituents and substitution patterns on the compounds of formula (I) can be selected by one of ordinary skill in the art to provide compounds that are chemically stable and that can be readily synthesized by techniques known in the art as well as those methods set forth herein.

The term “subject” as used herein, refers to an animal, preferably a mammal, most preferably a human, who has been the object of treatment, observation or experiment.

The term “therapeutically effective amount” as used herein, refers to an amount of an active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue system, animal or human that is being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation or partial alleviation of the symptoms of the disease, syndrome, condition, or disorder being treated.

As used herein, the term “composition” is intended to encompass a product comprising the specified ingredients in therapeutically effective amounts, as well as any product that results, directly or indirectly, from combinations of the specified ingredients in the specified amounts.

For the purposes of the present invention, the term “antagonist” is used to refer to a compound capable of producing, depending on the circumstance, a functional antagonism of an ion channel, including but not limited to competitive antagonists, non-competitive antagonists, desensitizing agonists, and partial agonists.

For the purposes of the present invention, the term “inflammatory hypersensitivity” is used to refer to a condition that is characterized by one or more hallmarks of inflammation, including edema, erythema, hyperthermia and pain, and/or by an exaggerated physiologic or pathophysiologic response to one or more than one type of stimulation, including thermal, mechanical and/or chemical stimulation.

For purposes of the present invention, the term “TRPM8-modulated” is used to refer to the condition of being affected by the modulation of the TRPM8 receptor, including but not limited to, the state of being mediated by the TRPM8 receptor.

Compounds of the present invention include those wherein:

-   -   a) A is CR⁵;     -   b) A is N; with the proviso that A is not N when G is S(O₂);     -   c) B is CR⁶;     -   d) B is N; with the proviso that B is not N when G is S(O₂);     -   e) A is CR⁵ and B is CR⁶;     -   f) A is CR⁵ and B is CH;     -   g) A is N and B is CR⁶; with the proviso that A is not N when G         is S(O₂);     -   h) A is N and B is CH; with the proviso that A is not N when G         is S(O₂);     -   i) B is N and A is CR⁵; with the proviso that B is not N when G         is S(O₂);     -   j) G is S;     -   k) G is S(O₂); and A and B are C(R⁵) and C(R⁶), respectively;     -   l) Y is H;     -   m) Y is isopropenyl;     -   n) Y is C₁₋₆ alkylcarbonyl optionally substituted with 1 chloro         substituent or 1 to 3 fluoro substituents;     -   o) Y is C₃₋₆ cycloalkylcarbonyl;     -   p) Y is phenylcarbonyl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl, fluoro, or         chloro;     -   q) Y is phenylcarbonyl substituted with trifluoromethyl and         optionally one additional substituent selected from         trifluoromethyl, chloro, fluoro, or C₁₋₄ alkyl;     -   r) Y is heteroaryl optionally substituted with one to two         substituents independently selected from chloro, fluoro, bromo,         trifluoromethyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄ alkyl, C₁₋₃         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, amino, C₁₋₃ alkylamino,         or di(C₁₋₃)alkylamino;     -   s) Y is benzo-fused heteroaryl optionally substituted with one         to two substituents independently selected from chloro, fluoro,         bromo, trifluoromethyl, C₁₋₄ alkyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, amino, C₁₋₃ alkylamino,         or di(C₁₋₃)alkylamino;     -   t) Y is bromo;     -   u) Y is chloro;     -   v) Y is fluoro;     -   w) Y is iodo;     -   x) Y is cyano;     -   y) Y is formyl;     -   z) Y is C₁₋₆ alkyl optionally substituted with 1 to 3         substituents independently selected from hydroxy, fluoro, or         chloro;     -   aa) Y is C(OH)(C₁₋₃ alkyl)₂;     -   bb) Y is C₃₋₆ cycloalkyl;     -   cc) Y is C₁₋₂ alkyl substituted with 1 substituent independently         selected from C₁₋₄ alkoxycarbonyl, cyano, C₁₋₃ alkylthio, C₁₋₄         alkoxy, or NR⁷R⁸ wherein R⁷ is hydrogen, C₁₋₄ alkyl, C₁₋₃         alkylcarbonyl, or C₁₋₃ alkylsulfonyl and R⁸ is hydrogen or C₁₋₄         alkyl; or R⁷ and R⁸ are taken together with the nitrogen atom to         which they are attached to form a 5 or 6 membered ring         optionally containing one additional heteroatom selected from         nitrogen, oxygen, or sulfur;     -   dd) Y is C₁₋₄ alkoxycarbonyl;     -   ee) Y is C₁₋₃ alkoxy;     -   ff) Y is hydroxy;     -   gg) Y is C₆₋₁₀ aryl optionally with one to three substituents         independently selected from chloro, fluoro, bromo, C₁₋₄ alkoxy,         hydroxy, C₁₋₃ alkoxycarbonyl, C₁₋₃ alkylthio, cyano, amino, C₁₋₂         alkylamino, di(C₁₋₂)alkylamino, or C₁₋₆ alkyl optionally         substituted with one to three halogen substituents; with the         proviso that not more than two of the substituents are selected         from the group consisting of C₁₋₃ alkoxycarbonyl, C₁₋₃         alkylthio, cyano, amino, C₁₋₂ alkylamino, di(C₁₋₂)alkylamino,         and C₁₋₆ alkyl substituted with one to three halogen         substituents;     -   hh) Y is NR⁹R¹⁰ wherein R⁹ is hydrogen, C₁₋₄ alkyl, C₁₋₃         alkylcarbonyl, or C₁₋₃ alkylsulfonyl and R¹⁰ is hydrogen or C₁₋₄         alkyl, or R⁹ and R¹⁰ are taken together with the nitrogen atom         to which they are attached to form a 5 or 6 membered ring         optionally containing one additional heteroatom selected from         nitrogen, oxygen, or sulfur; and wherein said 5 or 6 membered         ring is optionally substituted with a C₁₋₄ alkyl substituent;         with the proviso that when G is S and R¹⁰ is hydrogen, R⁹ is         other than hydrogen and C₁₋₄ alkyl;     -   ii) Y is aminocarbonyl;     -   jj) Y is methylaminocarbonyl;     -   kk) Y is dimethylaminocarbonyl;     -   ll) Y is arylhydroxy(C₁₋₃)alkyl;     -   mm) Y is hydrogen; isopropenyl; pyrimidinyl; thienyl; bromo;         chloro; fluoro; iodo; cyano; formyl; aminocarbonyl;         methylaminocarbonyl; dimethylaminocarbonyl; C₁₋₆alkylcarbonyl;         C₃₋₆ cycloalkyl; C₁₋₃ alkoxy; C₁₋₂alkyl optionally substituted         with 1 to 3 groups independently selected from hydroxy, C₁₋₄         alkoxy, fluoro, chloro, or NR⁷R⁸ wherein R⁷ is hydrogen, C₁₋₄         alkyl, C₁₋₃ carbonyl, or C₁₋₃ alkylsulfonyl and R⁸ is hydrogen         or C₁₋₄ alkyl or R⁷ and R⁸ are taken together with the nitrogen         atom to which they are attached to form a 5 or 6 membered ring         optionally containing one additional heteroatom selected from         nitrogen, oxygen, or sulfur; NR⁹R¹⁰ wherein R⁹ is C₁₋₄ alkyl,         C₁₋₃ alkylcarbonyl, or C₁₋₃ alkylsulfonyl and R¹⁰ is hydrogen or         C₁₋₄ alkyl, or R⁹ and R¹⁰ are taken together with the nitrogen         atom to which they are attached to form a 5 or 6 membered ring         optionally containing one additional heteroatom selected from         nitrogen, oxygen, or sulfur; and wherein said 5 or 6 membered         ring is optionally substituted with a C₁₋₄ alkyl substituent;         with the proviso that when G is S and R¹⁰ is hydrogen, R⁹ is         other than hydrogen and C₁₋₄ alkyl; or C₆₋₁₀ aryl optionally         substituted with 1 to three groups independently selected from         chloro, fluoro, or bromo; or Y is methylamino or dimethylamino         when G is S(O)₂;     -   nn) Y is hydrogen, isopropenyl, formyl, methyl, isopropyl,         trifluoromethyl, methoxy, chloro, acetyl, hydroxymethyl,         1-hydroxyethyl, 1-methoxyethyl, 1-hydroxy-1-methyl-ethyl,         methylamino-methyl, dimethylamino-methyl, n-propylamino-methyl,         pyrrolidin-1-ylmethyl, 4-methyl-piperazin-1-yl, piperazin-1-yl;         cyclopropyl, cyclobutyl, cyclopentyl, aminocarbonyl,         methylaminocarbonyl, dimethylaminocarbonyl, methylcarbonyl,         methanesulfonylamino, bromo, cyano, pyrimidin-5-yl, thien-3-yl,         2-fluorophenyl, or 4-fluorophenyl; or Y is methylamino or         dimethylamino when G is S(O)₂;     -   oo) Y is hydrogen, methyl, isopropyl, isopropenyl,         trifluoromethyl, methoxy, chloro, acetyl, hydroxymethyl,         1-hydroxyethyl, 1-methoxyethyl, 1-hydroxy-1-methyl-ethyl,         methylamino-methyl, dimethylamino-methyl, cyclopropyl,         cyclobutyl, cyclopentyl, aminocarbonyl, methylaminocarbonyl,         dimethylaminocarbonyl, methylcarbonyl, or bromo; or Y is         dimethylamino when G is SO₂;     -   pp) R¹ is C₆₋₁₀ aryl, wherein when C₆₋₁₀ aryl is phenyl,         substituted with carboxy at the 2 position, Y is chloro;     -   qq) R¹ is CF₃;     -   rr) R¹ is C₁₋₆ alkyl optionally substituted with 1 substituent         selected from C₁₋₃ alkylsulfonyl, C₁₋₄ alkoxycarbonyl, formyl,         hydroxy, carboxy, trifluoromethyl, C₁₋₄ alkoxy, C₁₋₃ alkylthio,         bromo, cyano, R¹¹, or R¹²;     -   ss) R¹ is aryl(C₁₋₂alkyl) wherein the ring of the aryl group is         optionally substituted with 1 to 3 substituents independently         selected from C₁₋₄ alkyl, fluoro, chloro, trifluoromethyl,         hydroxy, C₁₋₄ alkoxy, C₁₋₄ alkoxycarbonyl, or carboxy; with the         proviso that not more than two of the substituents are selected         from the group consisting of trifluoromethyl, C₁₋₄         alkoxycarbonyl, and carboxy;     -   tt) R¹ is heteroaryl(C₁₋₆ alkyl) wherein the heteroaryl group is         bound through a nitrogen heteroatom and is selected from         imidazolyl, triazolyl, or tetrazolyl; wherein the imidazolyl         group is optionally substituted with 1 substituent selected from         C₁₋₄ alkyl, trifluoromethyl, hydroxy, C₁₋₄ alkoxy, C₁₋₄         alkoxycarbonyl, carboxy, aminomethyl, methylamino-methyl, or         dimethylamino-methyl; and imidazolyl is optionally substituted         with one additional substitutent selected from fluoro and         chloro;     -   uu) R¹ is unsubstituted C₃₋₈cycloalkyl or cyclohexyl substituted         at the 4-position with one substituent selected from the group         consisting of cyano, C₁₋₄ alkoxycarbonyl, carboxy,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl, di(C₁₋₃         alkyl)aminocarbonyl, aminomethyl, methylamino-methyl,         dimethylamino-methyl, R¹¹, and R¹²;     -   vv) R¹ is benzo-fused C₅₋₆cycloalkyl attached at the benzo         portion of the ring system, and wherein the C₅₋₆cycloalkyl         portion of benzo-fused C₅₋₆cycloalkyl is optionally substituted         with amino, methylamino, or dimethylamino;     -   ww) phenyl substituted with 3- or 4-imidazolyl, wherein the         point of attachment of the imidazolyl is through a nitrogen         heteroatom; and wherein the imidazolyl is optionally         independently substituted with one to two substituents selected         from the group consisting of C₁₋₃ alkyl, 2-cyano, chloro, bromo,         amino-C₁₋₂ alkyl, (C₁₋₂ alkyl)amino-C₁₋₂ alkyl, and di(C₁₋₂         alkyl)amino-C₁₋₂ alkyl; wherein di(C₁₋₃ alkyl) is optionally         taken together with the nitrogen atom to which it is attached to         form a 5 or 6 membered ring optionally containing one additional         heteroatom selected from nitrogen, oxygen, or sulfur; and         wherein the ring formed by di(C₁₋₃ alkyl)amino is optionally         substituted with C₁₋₃alkyl; with the proviso that not more than         one of the substituents is amino-C₁₋₂ alkyl, (C₁₋₂         alkyl)amino-C₁₋₂ alkyl, or di(C₁₋₂ alkyl)amino-C₁₋₂ alkyl;     -   xx) R¹ is C₆₋₁₀ aryl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl optionally         substituted with one to three chloro or fluoro substituents,         chloro, fluoro, bromo, C₁₋₄ alkoxy, phenyloxy, heteroaryloxy         wherein the heteroaryl ring is a 6 membered ring containing         carbon ring members and 1 or 2 nitrogen heteroatom ring members,         C₁₋₃ alkylsulfonyl, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio,         hydroxy, carboxy, cyano, heteroaryl, C₁₋₃ alkylcarbonyl,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, P(O)(OC₁₋₃ alkyl)₂, P(O)(OH)₂, SO₃H,         C(O)NHOH, or SO₂NH₂; with the proviso that not more than two of         the substituents are selected from the group consisting of         phenyloxy, heteroaryloxy, C₁₋₃ alkylsulfonyl, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, hydroxy, carboxy, cyano,         heteroaryl, C₁₋₃ alkylcarbonyl, aminocarbonyl, C₁₋₃         alkylaminocarbonyl, di(C₁₋₃) alkylaminocarbonyl, and P(O)(OC₁₋₃         alkyl)₂ and not more than one of the substituents is selected         from the group consisting of —P(O)(OH)₂, —SO₃H, —C(O)NHOH, and         —SO₂NH₂;     -   yy) R¹ is phenyl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl optionally         substituted with one to three chloro or fluoro substituents or         one hydroxy substituent, chloro, fluoro, bromo, C₁₋₄ alkoxy,         trifluoromethoxy, 3- or 4-phenyloxy, 3- or 4-heteroaryloxy         wherein the heteroaryl ring is a 6 membered ring containing         carbon ring members and 1 or 2 nitrogen heteroatom ring members,         C₁₋₃ alkylsulfonyl, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio,         hydroxy, carboxy, cyano, nitro, 3- or 4-heteroaryl, C₁₋₃         alkylcarbonyl, aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃ alkylsulfonylaminocarbonyl,         di(C₁₋₃)alkylaminosulfonyl, P(O)(OC₁₋₃ alkyl)₂, P(O)(OH)₂, SO₃H,         C(O)NHOH, C(═N)NH₂, C(═NOH)NH₂, C(═N(methylcarbonyloxy))NH₂, or         SO₂NH₂; with the proviso that not more than two of the         substituents are selected from the group consisting of         trifluoromethoxy, 3- or 4-phenyloxy, 3- or 4-heteroaryloxy, C₁₋₃         alkylsulfonyl, C₁₋₄ alkoxycarbonyl, C₁₋₃alkylthio, carboxy,         cyano, 3- or 4-heteroaryl wherein the heteroaryl is other than         imidazolyl, C₁₋₃ alkylcarbonyl, aminocarbonyl, C₁₋₃         alkylaminocarbonyl, di(C₁₋₃) alkylaminocarbonyl, C₁₋₃         alkylsulfonylaminocarbonyl, and P(O)(OC₁₋₃ alkyl)₂ and not more         than one of the substituents is selected from the group         consisting of —P(O)(OH)₂, —SO₃H, carboxy, C(O)NHOH, C(═N)NH₂,         C(═NOH)NH₂, C(═N(C₁₋₃alkylcarbonyloxy))NH₂, and —SO₂NH₂; wherein         the phenyloxy is optionally substituted with one to two         substituents independently selected from the group consisting of         methyl and fluoro;         -   and wherein the heteroaryl substituent is optionally             independently substituted with one to two substituents             selected from the group consisting of C₁₋₄ alkyl,             trifluoromethyl, trifluoromethoxy, cyano, amino,             methylamino, dimethylamino, chloro, bromo, carboxy, C₁₋₂             alkoxycarbonyl, C₁₋₂ alkoxycarbonylmethyl, carboxymethyl,             amino-C₁₋₂ alkyl, (C₁₋₂ alkyl)amino-C₁₋₂ alkyl, and di(C₁₋₂             alkyl)amino-C₁₋₂ alkyl; with the proviso that not more than             one of the substituents is selected from the group             consisting of carboxy, C₁₋₂ alkoxycarbonyl, C₁₋₂             alkoxycarbonylmethyl, carboxymethyl, amino-C₁₋₂ alkyl, (C₁₋₂             alkyl)amino-C₁₋₂ alkyl, and di(C₁₋₂ alkyl)amino-C₁₋₂ alkyl;     -   zz) R¹ is naphthyl optionally substituted with one substituent         selected from the group consisting of hydroxy, chloro, fluoro,         bromo, C₁₋₄ alkoxycarbonyl, and carboxy;     -   aaa) R¹ is C₆₋₁₀ aryl substituted with phenyl optionally         substituted with one to two substituents selected from chloro,         fluoro, C₁₋₄ alkoxy, C₁₋₄ alkoxycarbonyl, carboxy, hydroxy,         amino, di(C₁₋₃)alkylamino, C₁₋₃ alkylamino, or C₁₋₃ alkyl;     -   bbb) R¹ is a ring selected from indanyl or tetralinyl wherein         said ring is attached via an unsaturated carbon atom and the         saturated portion of the ring is substituted with amino, (C₁₋₃         alkyl)amino, or di(C₁₋₃ alkyl)amino;     -   ccc) R¹ is phenyl substituted with R¹¹ or R¹² at the 3 or 4         position; and phenyl is optionally substituted with one         additional substituent selected from fluoro, chloro, or C₁₋₃         alkyl;     -   ddd) R¹ is pyridin-3-yl substituted at a carbon atom other than         that adjacent to the carbon bearing S(O)₂ with a substituent         selected from N-imidazolyl, oxadiazolyl, thiazolyl, R¹¹, or R¹²;         wherein pyridin-3-yl is optionally substituted with one         additional substituent selected from fluoro, chloro, or C₁₋₃         alkyl; and further, wherein the N-imidazolyl group is optionally         substituted with one to two substituents, and the oxadiazolyl         and thiazolyl groups are optionally substituted one substituent,         said substituent(s) independently selected from the group         consisting of C₁₋₄ alkyl, trifluoromethyl, cyano, amino,         methylamino, dimethylamino, chloro, bromo, carboxy, C₁₋₂         alkoxycarbonyl, C₁₋₂ alkoxycarbonylmethyl, carboxymethyl,         amino-C₁₋₂ alkyl, (C₁₋₂ alkyl)amino-C₁₋₂ alkyl, and di(C₁₋₂         alkyl)amino-C₁₋₂ alkyl; with the proviso that not more than one         of the substituents is selected from the group consisting of         carboxy, C₁₋₂ alkoxycarbonyl, C₁₋₂ alkoxycarbonylmethyl,         carboxymethyl, trifluoromethyl, cyano, amino-C₁₋₂ alkyl, (C₁₋₂         alkyl)amino-C₁₋₂ alkyl, and di(C₁₋₂ alkyl)amino-C₁₋₂ alkyl;     -   eee) R¹ is imidazolyl substituted with R¹¹ or R¹²; and         imidazolyl is optionally substituted at a nitrogen atom with         C₁₋₄ alkyl;     -   fff) R¹ is a ring selected from phenyl or pyridin-3-yl, wherein         said ring is substituted with NR¹⁵R¹⁶; wherein R¹⁵ is hydrogen,         C₁₋₄ alkyl, C₁₋₄ alkylcarbonyl, trifluoromethylcarbonyl,         trifluoromethylsulfonyl, C₃₋₆ cycloalkylsulfonyl, or C₁₋₃         alkylsulfonyl; and R¹⁶ is hydrogen or C₁₋₄ alkyl; or R¹⁵ and R¹⁶         are taken together with the nitrogen atom to which they are         attached to form a 5 or 6 membered ring optionally containing         one additional heteroatom selected from nitrogen, oxygen, or         sulfur optionally substituted with one or two oxo substituents;         and wherein the ring formed by NR¹⁵R¹⁶ is optionally substituted         with C₁₋₃alkyl, C₁₋₂ alkoxycarbonyl, or carboxy; and wherein         said phenyl is optionally substituted with one to two additional         substituents independently selected from the group consisting of         C₁₋₄ alkyl, C₁₋₄ alkoxy, hydroxy, fluoro, chloro, and bromo;     -   ggg) R¹ is phenyl substituted with C(O)NR¹⁷R¹⁸ wherein R¹⁷ is         hydrogen, C₁₋₄ alkyl, C₁₋₄ alkylcarbonyl, pyrrolidin-3-yl, or         C₁₋₃ alkylsulfonyl; and R¹⁸ is hydrogen or C₁₋₄ alkyl; or R¹⁷         and R¹⁸ are taken together with the nitrogen atom to which they         are attached to form a 5 or 6 membered ring optionally         containing one additional heteroatom selected from nitrogen,         oxygen, or sulfur; and wherein said ring is optionally         substituted with C₁₋₃alkyl;     -   hhh) R¹ is phenyl substituted with 4 or 5 fluoro substituents;     -   iii) R¹ is phenyl substituted at the 4-position with         -Q-C(R^(x)R^(y))—(CH₂)₀₋₁CO₂H wherein Q is a bond or O; and         wherein R^(x) and R^(y) are independently hydrogen or methyl; or         R^(x) and R^(y) are taken together with the carbon atom to which         they are both attached to form a cyclopropyl ring;     -   jjj) R¹ is heteroaryl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl, chloro,         fluoro, bromo, trifluoromethyl, C₁₋₄ alkoxy, oxo, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, carboxy, amino, C₁₋₃         alkylamino, or di(C₁₋₃)alkylamino; with the proviso that not         more than two of the substituents are selected from the group         consisting of trifluoromethyl, C₁₋₄ alkoxy, oxo, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, carboxy, amino, C₁₋₃         alkylamino, and di(C₁₋₃)alkylamino;     -   kkk) R¹ is benzo-fused heteroaryl optionally substituted with         one to three substituents independently selected from C₁₋₄         alkyl, chloro, fluoro, bromo, trifluoromethyl, C₁₋₄ alkoxy, oxo,         hydroxy, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio, cyano, carboxy,         amino, C₁₋₃ alkylamino, or di(C₁₋₃)alkylamino; with the proviso         that not more than two of the substituents are selected from the         group consisting of trifluoromethyl, C₁₋₄ alkoxy, oxo, hydroxy,         C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio, cyano, carboxy, amino, C₁₋₃         alkylamino, and di(C₁₋₃)alkylamino;     -   lll) R¹ is benzo-fused heterocycle optionally substituted with         one to two substituents independently selected from         trifluoromethyl, C₁₋₃ alkylcarbonyl, C₁₋₄ alkyl, C₁₋₄ alkoxy,         trifluoromethylcarbonyl, fluoro, chloro, bromo, hydroxy, oxo,         carboxy, or C₁₋₄ alkoxycarbonyl; such that when the benzo-fused         heterocycle is substituted on the heterocyclic ring, the         substituents on the heterocyclic ring are selected from oxo,         hydroxy, C₁₋₄ alkyl, or trifluoromethylcarbonyl; with the         proviso that not more than one substituent is         trifluoromethylcarbonyl; and with the proviso that when the         benzo-fused heterocycle is substituted with         trifluoromethylcarbonyl, at least one of the ring members of the         heterocycle is a nitrogen heteroatom and the point of attachment         to the trifluoromethylcarbonyl substituent is through the         nitrogen heteroatom;     -   mmm) R¹ is amino;     -   nnn) R¹ is C₁₋₆alkylamino;     -   ooo) R¹ is di(C₁₋₆ alkyl)amino;     -   ppp) R¹ is C₁₋₆ alkyl optionally substituted with 1 substituent         selected from the group consisting of C₁₋₃ alkylsulfonyl, C₁₋₃         alkoxycarbonyl, hydroxy, carboxy, formyl, trifluoromethyl,         bromo, and a 5 to 6 membered heteroaryl optionally substituted         with C₁₋₄ alkyl, aminomethyl, methylamino-methyl, or         dimethylamino-methyl;     -   qqq) R¹ is methyl, ethyl, propyl, butyl, phenylmethyl,         carboxymethyl, methoxycarbonylmethyl, 2-(methoxycarbonyl)ethyl,         2,2,2-trifluoroethyl, 2-bromoethyl, 2-hydroxyethyl,         2-formylethyl, 2-carboxyethyl, 3-bromopropyl, 3-hydroxypropyl,         3-(methoxycarbonyl)propyl, 3-(imidazol-1-yl)propyl,         4-(imidazol-1-yl)butyl, 3-hydroxy-3-methyl-butyl, 4-bromobutyl,         4-hydroxybutyl, 4-(4-methyl-piperazin-1-yl)butyl,         4-hydroxy-4-methylpentyl, or methanesulfonylmethyl;     -   rrr) R¹ is phenyl optionally substituted with one to three         substituents independently selected from hydroxy, fluoro,         chloro, bromo, cyano, nitro, 3- or 4-heteroaryl, 3- or         4-phenyloxy, 3- or 4-heteroaryloxy, C₁₋₃         alkylsulfonylaminocarbonyl, di(C₁₋₃)alkylaminosulfonyl,         C(═NOH)NH₂, C(O)NHOH, C(C═N(methylcarbonyloxy))NH₂,         aminocarbonyl, C₁₋₄ alkyl substituted with one to three chloro         or fluoro substituents or one hydroxy substituent,         C₁₋₃alkylcarbonyl, C₁₋₃alkoxycarbonyl, C₁₋₃ alkoxy, or carboxy;         wherein the phenyloxy is optionally substituted with one to two         substituents independently selected from the group consisting of         methyl and fluoro;     -   sss) R¹ is phenyl optionally substituted with one to three         substituents independently selected from C₁₋₄ alkyl optionally         substituted with one hydroxy substituent, hydroxy, fluoro,         bromo, cyano, nitro, thiadazolyl, pyrazol-1-yl,         2-methyl-pyrimidin-4-yl, oxazol-5-yl, 1H-tetrazol-5-yl,         2H-tetrazol-5-yl, 1H-tetrazol-5-yl, 3- or 4-phenyloxy, 3- or         4-pyridinyloxy, methanesulfonylaminocarbonyl,         di(methyl)aminosulfonyl, C(═NOH)NH₂, C(O)NHOH,         C(C═N(methylcarbonyloxy))NH₂, trifluoromethyl, methoxycarbonyl,         aminocarbonyl, methoxy, or carboxy; wherein the phenyloxy is         optionally substituted with a fluoro substituent;     -   ttt) R¹ is phenyl substituted with R¹¹ or R¹² at the 3 or 4         position; and optionally one additional substituent selected         from fluoro, chloro, or C₁₋₃ alkyl;     -   uuu) R¹ is phenyl, 3-cyanophenyl, 4-cyanophenyl,         2,5-dibromophenyl, 4-bromophenyl, 4-nitrophenyl,         3-hydroxyphenyl, 4-hydroxyphenyl,         4-(1-hydroxy-1-methyl-ethyl)phenyl, phenyl,         4-hydroxy-3-fluorophenyl, 4-[1,2,3]thiadiazol-4-ylphenyl,         4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)phenyl,         4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl,         4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl,         4-(5-oxo-4,5-dihydro-1H-[1,2,4]triazol-3-yl)phenyl,         4-(1-methyl-5-oxo-4,5-dihydro-1H-[1,2,4]triazol-3-yl)-phenyl,         3-(5-methyl-[1,3,4]oxadiazol-2-yl)phenyl, 3-phenoxyphenyl,         3-fluoro-4-(phenylmethoxy)phenyl,         3-fluoro-4-(4-fluorophenylmethoxy)phenyl,         4-pyridin-3-yloxyphenyl, 4-pyridin-4-yloxyphenyl,         3-fluorophenyl, 2-fluorophenyl, 4-perfluoromethylphenyl,         4-methoxycarbonylphenyl, 4-methylcarbonylphenyl,         3-methoxycarbonylphenyl, 2-methoxycarbonylphenyl,         3-dimethylaminosulfonylphenyl,         4-(methanesulfonylaminocarbonyl)phenyl, 4-fluorophenyl,         3,4-difluorophenyl, 4-methoxyphenyl, 4-aminocarbonyl,         4-carboxyphenyl, 3-carboxyphenyl, 2-carboxyphenyl,         4-(2-dimethylaminomethyl-imidazol-1-yl)phenyl,         4-(N-hydroxy-acetamidinyl)phenyl, 4-hydroxyaminocarbonylphenyl,         4-(N-(methylcarbonyloxy)acetamidinyl)phenyl,         4-(pyrazol-1-yl)phenyl, 3-(2-methyl-pyrimidin-4-yl)phenyl,         4-(oxazol-5-yl)phenyl, 3-(1H-tetrazol-5-yl)phenyl,         3-(2H-tetrazol-5-yl)phenyl, 4-(1H-tetrazol-5-yl)phenyl, or         3-methoxyphenyl;     -   vvv) R¹ is 2-aminoindan-5-yl;     -   www) R¹ is pyridin-3-yl substituted with         5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl or 1H-tetrazol-5-yl;     -   xxx) R¹ is a ring selected from phenyl or pyridin-3-yl wherein         said ring is substituted with NR¹⁵R¹⁶; wherein R¹⁵ is hydrogen,         C₁₋₄ alkyl, methylcarbonyl, trifluoromethylcarbonyl,         cyclopropylsulfonyl, or C₁₋₃ alkylsulfonyl; and R¹⁶ is hydrogen         or C₁₋₄ alkyl; or R¹⁵ and R¹⁶ are taken together with the         nitrogen atom to which they are attached to form morpholin-4-yl,         piperazin-1-yl, piperadin-1-yl, thiomorpholin-4-yl, or         pyrrolidin-1-yl; and wherein the ring formed by NR¹⁵R¹⁶ is         optionally substituted with C₁₋₃alkyl; and wherein said phenyl         is optionally substituted with one to two additional         substituents independently selected from the group consisting of         methoxy, hydroxy, chloro, and bromo;     -   yyy) R¹ is phenyl substituted with C(O)NR¹⁷R¹⁸ wherein R¹⁷ is         hydrogen, C₁₋₄ alkyl, pyrrolidin-3-yl, or C₁₋₃ alkylsulfonyl;         and R¹⁸ is hydrogen; or R¹⁷ and R¹⁸ are taken together with the         nitrogen atom to which they are attached to form         4-methyl-piperazin-1-yl;     -   zzz) R¹ is pyridinyl, quinolinyl, quinoxalinyl,         imidazo[2,1-b]thiazol-5-yl, thienyl, imidazolyl,         benzothiophenyl, benzothiazolyl, benzooxazolyl, isoxazolyl,         isoquinolinyl, benzooxazinyl, thiadiazolyl, furanyl, thiazolyl,         pyrazolyl, imidazolyl, benzoxadiazolyl, benzothiadiazolyl,         benzimidazolyl, pyrimidinyl, or furanyl, any of which can be         optionally substituted with one to three substituents         independently selected from C₁₋₃ alkyl, C₁₋₃ alkoxy, hydroxy,         oxo, chloro, bromo, trifluoromethyl, C₁₋₃ alkoxycarbonyl, C₁₋₃         alkylthio, di(C₁₋₃)alkylamino, or heteroaryl selected from the         group consisting of 1H-tetrazol-5-yl, isoxazolyl, and pyrazolyl;         wherein the heteroaryl other than tetrazol-5-yl is optionally         independently substituted with one to two substituents selected         from the group consisting of C₁₋₃ alkyl, chloro, and         trifluoromethyl; with the proviso that not more than two of the         substituents are selected from the group consisting of hydroxy,         heteroaryl, and oxo;     -   aaaa) R¹ is pyridinyl, quinolinyl, quinoxalinyl,         imidazo[2,1-b]thiazol-5-yl, thienyl, imidazolyl,         benzothiophenyl, benzothiazolyl, benzimidazolyl, furanyl,         isoquinolinyl, thiazolyl, pyrazolyl, imidazolyl, or pyrimidinyl,         any of which can be optionally substituted with one to three         substituents independently selected from C₁₋₃ alkyl, methoxy,         hydroxy, oxo, chloro, bromo, trifluoromethyl, methoxycarbonyl,         carboxy, methylthio, dimethylamino, or heteroaryl selected from         the group consisting of 1H-tetrazol-5-yl, isoxazolyl, and         pyrazolyl; wherein the heteroaryl other than tetrazol-5-yl is         optionally independently substituted with one to two         substituents selected from the group consisting of C₁₋₃ alkyl,         chloro, and trifluoromethyl; with the proviso that not more than         two of the substituents are selected from the group consisting         of hydroxy, heteroaryl, and oxo;     -   bbbb) R¹ is tetrahydroisoquinolinyl, dihydrobenzooxazinyl,         tetrahydropyrimidinyl, or dihydrobenzooxazolyl, any of which can         be optionally substituted with one to two substituents         independently selected from C₁₋₄ alkyl, trifluoromethylcarbonyl,         or oxo; with the proviso that not more than one substituent is         trifluoromethylcarbonyl and the point of attachment to the         trifluoromethylcarbonyl substituent is through a nitrogen         heteroatom;     -   cccc) R¹ is 1-methyl-1H-imidazol-4-yl, pyridin-3-yl,         6-(1H-tetrazol-5-yl)pyridin-3-yl, 2-chloropyridin-3-yl,         6-chloropyridin-3-yl, 6-dimethylaminopyridin-3-yl,         2-dimethylaminopyridin-3-yl, 6-methoxypyridin-3-yl,         2-methoxypyridin-3-yl, 5-bromo-6-chloropyridin-3-yl,         5,6-dichloropyridin-3-yl, 6-methylthiopyridin-3-yl,         2-methylthiopyridin-3-yl, quinoxalin-5-yl, thien-2-yl,         thien-3-yl, 4-carboxythien-2-yl, 5-carboxy-3-methyl-thien-2-yl,         5-(5-trifluoromethyl-isoxazol-3-yl)-thien-2-yl,         5-(2-methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-thien-2-yl,         6-chloro-imidazo[2,1-b]thiazol-5-yl, benzo[b]thiophen-2-yl,         quinolin-8-yl, 8-methoxyquinolin-5-yl, isoquinolin-5-yl,         benzothiazol-6-yl, benzimidazol-2-yl, 1-methylbenzimidazol-2-yl,         5-chloro-1-methyl-benzimidazol-2-yl,         2-oxo-2,3-dihydro-benzooxazol-6-yl,         4-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl,         2,4-dihydroxy-6-methylpyrimidin-5-yl,         2-(2,2,2-trifluoro-acetyl)-1,2,3,4-tetrahydro-isoquinolin-8-yl,         2-(2,2,2-trifluoro-acetyl)-1,2,3,4-tetrahydro-isoquinolin-7-yl,         2-methyl-1,2,3,4-tetrahydro-isoquinolin-7-yl,         1,3,5-trimethyl-1H-pyrazol-4-yl,         1-methyl-3-trifluoromethyl-1H-pyrazol-4-yl,         5-methoxycarbonylfuran-2-yl, 5-carboxyfuran-2-yl,         2,4-dimethyl-thiazol-5-yl, 1,2,3,4-tetrahydro-isoquinolin-8-yl,         or 2-chloropyridin-5-yl;     -   dddd) R¹ is 1-methyl-1H-imidazol-4-yl, pyridin-3-yl,         6-(1H-tetrazol-5-yl)pyridin-3-yl, 2-chloropyridin-3-yl,         2-chloropyridin-5-yl, 6-chloropyridin-3-yl,         6-dimethylaminopyridin-3-yl, 2-dimethylaminopyridin-3-yl,         6-methoxypyridin-3-yl, 2-methoxypyridin-3-yl,         5-bromo-6-chloropyridin-3-yl, 5,6-dichloropyridin-3-yl,         6-methylthiopyridin-3-yl, quinoxalin-5-yl, thien-2-yl,         thien-3-yl, 4-carboxythien-2-yl, 5-carboxy-3-methyl-thien-2-yl,         6-chloro-imidazo[2,1-b]thiazol-5-yl, benzo[b]thiophen-2-yl,         quinolin-8-yl, 8-methoxyquinolin-5-yl, isoquinolin-5-yl,         2-methyl-1,2,3,4-tetrahydro-isoquinolin-7-yl, benzothiazol-6-yl,         benzimidazol-2-yl, 2-oxo-2,3-dihydro-benzooxazol-6-yl,         4-methyl-3,4-dihydro-2H-benzo[1,4]oxazin-7-yl,         2,4-dihydroxy-6-methylpyrimidin-5-yl,         1,3,5-trimethyl-1H-pyrazol-4-yl,         1-methyl-3-trifluoromethyl-1H-pyrazol-4-yl,         5-methoxycarbonylfuran-2-yl, 2,4-dimethyl-thiazol-5-yl,         1,2,3,4-tetrahydro-isoquinolin-8-yl, or         2-(2,2,2-trifluoro-acetyl)-1,2,3,4-tetrahydro-isoquinolin-8-yl;     -   eeee) R¹ is thienyl optionally independently substituted with         one to two substituents selected from the group consisting of         methyl or carboxy; imidazolyl optionally substituted with 1         methyl substituent; pyridinyl optionally substituted with         1H-tetrazol-5-yl, dimethylamino, chloro, methoxy, or methylthio,         and optionally substituted with one additional bromo or chloro         substituent; furanyl optionally substituted with 1         methoxycarbonyl substituent; quinolinyl optionally substituted         with 1 methoxy substituent; isoquinolinyl; benzothiophenyl;         imidazo[2,1-b]thiazol-5-yl optionally substituted with 1 chloro         substituent; benzothiazolyl; benzimidazol-2-yl;         dihydrobenzooxazolyl optionally substituted with one oxo         substituent; dihydrobenzooxazinyl optionally substituted with         one substituent selected from methyl or oxo; pyrimidinyl         optionally substituted with from one to three substituents         independently selected from oxo or hydroxy;         tetrahydroisoquinolinyl optionally substituted on a nitrogen         heteroatom with a trifluoromethylcarbonyl substituent; or         pyrazolyl optionally substituted with from one to three         substituents selected from methyl or trifluoromethyl with the         proviso that not more than 1 substituent is trifluoromethyl;     -   ffff) R¹ is amino, methylamino, or dimethylamino;     -   gggg) R² is C₁₋₂ alkyl substituted with adamantyl;     -   hhhh) R² is C₁₋₆ alkyl substituted with two C₆₋₁₀ aryl groups         wherein one of said aryl groups is optionally substituted with 1         to 3 substituents independently selected from chloro, fluoro,         bromo, C₁₋₄ alkyl, C₁₋₄ alkoxy optionally substituted with 1 to         3 fluoro substituents, hydroxy, C₁₋₄ alkoxycarbonyl, C₁₋₃         alkylthio, cyano, trifluoromethyl, aminocarbonyl, C₁₋₃         alkylaminocarbonyl, di(C₁₋₃)alkylaminocarbonyl,         C₁₋₃alkylsulfonyl optionally substituted with 1 to 3 fluoro         substituents, nitro, amino, C₁₋₃ alkylamino, di(C₁₋₃)alkylamino,         or C₁₋₃ alkylcarbonyl; with the proviso that not more than two         of the substituents are selected from the group consisting of         C₁₋₄ alkoxy substituted with 1 to 3 fluoro substituents, C₁₋₄         alkoxycarbonyl, C₁₋₃alkylthio, cyano, trifluoromethyl,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃ alkylsulfonyl optionally         substituted with 1 to 3 fluoro substituents, nitro, amino, C₁₋₃         alkylamino, di(C₁₋₃)alkylamino, and C₁₋₃ alkylcarbonyl; and the         other of said aryl groups is optionally substituted with 1         substituent selected from chloro, fluoro, bromo, C₁₋₄ alkyl,         C₁₋₄ alkoxy optionally substituted with 1 to 3 fluoro         substituents, hydroxy, C₁₋₄ alkoxycarbonyl, C₁₋₃alkylthio,         cyano, trifluoromethyl, aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃alkylsulfonyl optionally         substituted with 1 to 3 fluoro substituents, nitro, amino,         C₁₋₃alkylamino, di(C₁₋₃)alkylamino, or C₁₋₃ alkylcarbonyl;     -   iiii) R² is C₁₋₆ alkyl substituted with one C₆₋₁₀ aryl group and         optionally one additional substituent selected from hydroxy or         oxo, wherein said C₆₋₁₀ aryl group is optionally substituted         with 1 to 3 substituents independently selected from chloro,         fluoro, bromo, C₁₋₄ alkyl, C₁₋₄ alkoxy optionally substituted         with 1 to 3 fluoro substituents, hydroxy, C₁₋₄ alkoxycarbonyl,         C₁₋₃ alkylthio, trifluoromethylthio, cyano, trifluoromethyl,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl,         di(C₁₋₃)alkylaminocarbonyl, C₁₋₃ alkylsulfonyl optionally         substituted with 1 to 3 fluoro substituents, nitro, amino, C₁₋₃         alkylamino, di(C₁₋₃)alkylamino, or C₁₋₃ alkylcarbonyl; with the         proviso that not more than two of the substituents are selected         from the group consisting of C₁₋₄ alkoxy substituted with 1 to 3         fluoro substituents, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio,         trifluoromethylthio, cyano, trifluoromethyl, aminocarbonyl, C₁₋₃         alkylaminocarbonyl, di(C₁₋₃)alkylaminocarbonyl, C₁₋₃         alkylsulfonyl optionally substituted with 1 to 3 fluoro         substituents, nitro, amino, C₁₋₃ alkylamino, di(C₁₋₃)alkylamino,         and C₁₋₃ alkylcarbonyl;     -   jjjj) R² is C₁₋₆ alkyl substituted with phenyl, wherein phenyl         is substituted with 4 or 5 fluoro substituents; or phenyl is         substituted with methoxy and 3 to 4 fluoro substituents;     -   kkkk) R² is C₁₋₆ alkyl substituted with one heteroaryl group and         optionally one additional substituent selected from oxo or         hydroxy wherein said heteroaryl group is optionally substituted         with one to three fluoro substituents or 1 substituent selected         from chloro, bromo, trifluoromethyl, C₁₋₄ alkoxy, hydroxy, C₁₋₄         alkoxycarbonyl, C₁₋₃ alkylthio, cyano, or C₁₋₄ alkyl;     -   llll) R² is C₁₋₆ alkyl substituted with one benzo-fused         heteroaryl group and optionally one additional substituent         selected from oxo or hydroxy, wherein said benzo-fused         heteroaryl group is optionally substituted with 1 substituent         selected from chloro, fluoro, bromo, trifluoromethyl, C₁₋₄         alkoxy, hydroxy, C₁₋₄ alkoxycarbonyl, C₁₋₃ alkylthio, cyano, or         C₁₋₄ alkyl;     -   mmmm) R² is C₁₋₆ alkyl substituted with one heterocycle group         wherein said heterocycle group is optionally substituted with         one to three substituents independently selected from C₁₋₄         alkyl, C₁₋₄ alkoxycarbonyl, oxo, or hydroxy; with the proviso         that not more than two of the substituents are selected from the         group consisting of oxo and hydroxy;     -   nnnn) R² is C₁₋₆ alkyl substituted with benzo[1,3]dioxol-5-yl,         2,2-difluoro-benzo[1,3]dioxol-5-yl, or         2,3-dihydro-benzo[1,4]dioxin-6-yl;     -   oooo) R² is C₂₋₆ alkyl optionally substituted with 1 to 2         substituents independently selected from cyano, trifluoromethyl,         C₁₋₆ alkylcarbonyl, C₁₋₆ alkylthio, C₁₋₆ alkylsulfonyl, amino,         C₁₋₃ alkylamino, di(C₁₋₃)alkylamino, C₂₋₆ alkenyl, C₂₋₆ alkynyl,         fluoro, C₁₋₆alkoxy, C₁₋₆alkoxycarbonyl, C₁₋₄         alkoxycarbonylamino, hydroxy, P(O)(OC₁₋₃)₂, C₃₋₆ cycloalkyloxy,         C₃₋₄ cycloalkyl, or C₅₋₈ cycloalkyl optionally substituted with         one to three substituents independently selected from the group         consisting of halogen, hydroxy, oxo and C₁₋₄ alkyl optionally         substituted with one to three substituents independently         selected from halogen or hydroxy; with the proviso that not more         than one of the substituents on the C₁₋₄ alkyl of the C₁₋₄ alkyl         substituted C₅₋₈ cycloalkyl is hydroxy, and not more than two of         the substituents on the C₅₋₈ cycloalkyl are oxo;     -   pppp) R² is C₁₋₆ alkyl substituted with one substituent selected         from cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl;     -   qqqq) R² is cyclopropylmethyl, cyclobutylmethyl,         cyclopentylmethyl, 2-(cyclopropyl)ethyl, or cyclohexylmethyl;     -   rrrr) R² is C₁₋₆ alkyl substituted with one substituent selected         from pyrrolidinyl, imidazolidinyl, morpholinyl,         tetrahydropyranyl, or piperidinyl; any of which is optionally         substituted with from one to three substituents independently         selected from C₁₋₄ alkyl, C₁₋₄ alkoxycarbonyl, or oxo; with the         proviso that not more than two of the substituents are oxo;     -   ssss) R² is 2-(2-oxo-pyrrolidin-1-yl)-ethyl,         (N-tert-butoxycarbonylpyrrolidinyl)methyl,         (2,5-dioxo-pyrrolidin-1-yl)-ethyl, morpholin-4-yl-ethyl,         tetrahydropyran-4-ylmethyl, 2-(piperidin-1-yl)ethyl,         2-(morpholin-4-yl)ethyl,         (N-tert-butoxycarbonylpyrrolidinyl)methyl,         5-oxo-pyrrolidin-2-ylmethyl, 2-(morpholin-4-yl)ethyl,         (N-tert-butoxycarbonylpyrrolidinyl)methyl,         2-(2-oxo-imidazolidin-1-yl)ethyl, 2-(piperidin-1-yl)ethyl,         5-oxo-pyrrolidin-2-ylmethyl, pyrrolidin-2-ylmethyl, or         piperidin-4-ylmethyl;     -   tttt) R² is C₁₋₆ alkyl substituted with phenyl optionally         substituted with one to three substituents independently         selected from C₁₋₄ alkyl, trifluoromethyl, C₁₋₄ alkoxy         optionally substituted with 1 to 3 fluoro substituents,         C₁₋₃alkylthio, trifluoromethylthio, C₁₋₃ alkoxycarbonyl,         aminocarbonyl, C₁₋₃ alkylaminocarbonyl, di(C₁₋₃)         alkylaminocarbonyl, C₁₋₄ alkylsulfonyl optionally substituted         with 1 to 3 fluoro substituents, chloro, fluoro, bromo, hydroxy,         or nitro with the proviso that not more than two of the         substituents are selected from the group consisting of         trifluoromethyl, C₁₋₄ alkoxy substituted with 1 to 3 fluoro         substituents, C₁₋₃ alkylthio, trifluoromethylthio, C₁₋₃         alkoxycarbonyl, aminocarbonyl, C₁₋₃ alkylaminocarbonyl, di(C₁₋₃)         alkylaminocarbonyl; C₁₋₄ alkylsulfonyl optionally substituted         with 1 to 3 fluoro substituents, and nitro;     -   uuuu) R² is C₁₋₆ alkyl substituted with phenyl optionally         substituted with one to two substituents independently selected         from methoxy, fluoro, nitro, trifluoromethoxy, trifluoromethyl,         methylthio, trifluoromethylthio, methoxycarbonyl,         methylsulfonyl, trifluoromethylsulfonyl, methyl, chloro, bromo,         or hydroxy;     -   vvvv) R² is 3-methoxyphenylmethyl, 4-methoxyphenylmethyl,         2-fluorophenylmethyl, 3-fluorophenylmethyl,         4-fluorophenylmethyl, 3,4,5-trifluorophenylmethyl,         3,4-difluorophenylmethyl, 2-nitrophenylmethyl,         2-trifluoromethoxyphenylmethyl, 3-trifluoromethoxyphenylmethyl,         4-trifluoromethoxyphenylmethyl, 4-difluoromethoxyphenylmethyl,         4-chloro-2-fluoro-5-methoxyphenylmethyl, phenylmethyl,         4-fluoro-3-trifluoromethylphenylmethyl,         4-fluoro-2-trifluoromethylphenylmethyl, 2-methylphenylmethyl,         3-methylphenylmethyl, 2,5-dichlorophenylmethyl,         3-chloro-4-fluorophenylmethyl, 4-chloro-3-fluorophenylmethyl,         2-(phenyl)ethyl, 4-chlorophenylmethyl, 2-methoxyphenylmethyl,         5-bromo-2-methoxyphenylmethyl, 3-methoxyphenylmethyl,         4-fluoro-3-methoxyphenylmethyl, 2-bromo-5-methoxyphenylmethyl,         4-methoxy-3-bromophenylmethyl, 3-nitrophenylmethyl,         3-methoxycarbonylphenylmethyl, 4-methoxycarbonylphenylmethyl,         4-trifluoromethylthiophenylmethyl,         4-trifluoromethylsulfonylphenylmethyl, or 3-hydroxyphenylmethyl;     -   wwww) R² is C₁₋₆ alkyl substituted with one substituent selected         from pyridinyl, benzo[1,3]dioxol-5-ylmethyl,         2,2-difluoro-benzo[1,3]dioxol-5-ylmethyl, or quinolinyl; wherein         said pyridinyl is optionally substituted with one to three         fluoro substitutents or 1 substituent selected from chloro,         bromo, trifluoromethyl, C₁₋₄alkoxy, hydroxy, C₁₋₄alkoxycarbonyl,         C₁₋₃ alkylthio, cyano, or C₁₋₄ alkyl;     -   xxxx) R² is quinolin-8-ylmethyl, benzo[1,3]dioxol-5-ylmethyl,         2,2-difluoro-benzo[1,3]dioxol-5-ylmethyl, pyridin-2-ylmethyl,         pyridin-3-ylmethyl, pyridin-4-ylmethyl,         2,3,6-trifluoro-pyridin-4-ylmethyl, or         2-fluoro-pyridin-4-ylmethyl;     -   yyyy) R² is C₁₋₂ alkyl substituted with adamantyl; or R² is C₁₋₆         alkyl optionally substituted with 1 to 2 substituents         independently selected from C₁₋₆ alkoxy; C₁₋₄         alkoxycarbonylamino; di(C₁₋₃)alkylamino; C₁₋₆ alkylsulfonyl;         C₁₋₆ alkylthio; fluoro; C₂₋₆ alkenyl; C₁₋₆ alkoxycarbonyl;         hydroxy; trifluoromethyl; C₂₋₆ alkynyl; C₁₋₆ alkylcarbonyl;         P(O)(OC₁₋₃)₂; C₃₋₆ cycloalkyloxy; or amino;     -   zzzz) R² is ethyl, 2-(tertbutoxy)ethyl, propyl, butyl, isobutyl,         pentyl, hexyl, allyl, 2-(tert-butoxycarbonylamino)ethyl,         2-(dimethylamino)ethyl, 2-(methanesulfonyl)ethyl,         2-(methoxycarbonyl)-2(R)-methylethyl,         2-(methoxycarbonyl)-2(S)-methylethyl, 2-(methylsulfanyl)ethyl,         methoxycarbonylmethyl, 2-methoxyethyl, 3-methoxy-3-methyl-butyl,         3,3,3,-trifluoropropyl, 4,4,4-trifluorobutyl,         5,5,5-trifluoropentyl, pent-3-ynyl, 2-fluoroethyl,         3-fluoropropyl, 2,2-difluoroethyl, 2-cyclohexyloxy-ethyl,         2-t-butoxyethyl, 3-t-butoxypropyl, 5-(ethoxycarbonyl)pentyl,         2(R),3-dihydroxypropyl, 2(S)-methoxycarbonyl-2-methylethyl,         2(R)-methoxycarbonyl-2-methylethyl, or 3-(methylcarbonyl)propyl;     -   a5) R³ is hydrogen;     -   b5) R³ is C₁₋₆ alkyl;     -   c5) R³ is trifluoromethyl;     -   d5) R³ is C₁₋₄ alkoxy;     -   e5) R³ is bromo;     -   f5) R³ is chloro;     -   g5) R³ is fluoro;     -   h5) R³ is hydroxy;     -   i5) R⁴ is hydrogen;     -   j⁵) R⁴ is fluoro;     -   k5) R⁴ is chloro;     -   l5) R⁴ is methyl;     -   m5) R⁵ is hydrogen;     -   n5) R⁶ is hydrogen,     -   o5) R⁶ is fluoro,     -   p5) R⁶ is chloro,     -   q5) R⁶ is methoxy,     -   r5) R⁶ is methyl;     -   s5) R¹¹ is selected from

-   -   t5) R¹² is selected from

wherein R¹³ is H, —C₁₋₄ alkyl, —CH₂NH(C₁₋₃alkyl), —CH₂NH(C₁₋₃alkyl)₂, or —CH₂CO₂H; and R¹⁴ is —C₁₋₂ alkyl, —C₁₋₃ alkyl-OH, or —C₁₋₃alkylCO₂H;

and any combination of embodiments a) through t5) above, provided that it is understood that combinations in which different embodiments of the same substituent would be combined are excluded; and with the proviso that when R¹ is C₆₋₁₀ aryl, wherein C₆₋₁₀ aryl is phenyl, substituted with carboxy at the 2 position, Y is not hydrogen; when R² is C₁₋₆ alkyl substituted with at least one P(O)(OCH₃)₂ substituent, R¹ is optionally substituted C₆₋₁₀ aryl; when R² is C₁₋₆ alkyl substituted with at least one C₁₋₆ alkoxycarbonyl substituent, R¹ is optionally substituted C₆₋₁₀ aryl; when Y is unsubstituted phenyl, and R¹ is ethyl, R² is not 4-fluoro-3-trifluoromethyphenylmethyl; when R² is C₁₋₆ alkyl substituted with an unsubstituted heterocycle comprising at least one nitrogen heteroatom, the point of attachment to the pendant group is through a nitrogen heteroatom; when R² is substituted or unsubstituted C₁₋₆ alkyl, R¹ is other than phenyl substituted at the 3-position with R¹¹ or R¹²;

-   with the proviso that Formula (I) is other than a compound selected     from the group consisting of -   a compound wherein G is S, Y is H, R¹ is 4-cyanophenyl, R² is     4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and     B is CR⁶; -   a compound wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is     octahydro-quinolizin-1-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A     is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is 1-hydroxyethyl, R¹ is     2,2,2-trifluoroethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl,     R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is methyl, R¹ is     4-piperazin-1-ylcarbonylphenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴,     R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is methylcarbonylamino, R¹ is     4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A     is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is H, R¹ is 3-aminocarbonylphenyl, R²     is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are     hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is bromo, R¹ is     4-(1-hydroxy-1-methyl-ethyl)phenyl, R² is     4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are     hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is methylaminocarbonyl, R¹ is     4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A     is CR⁵, and B is CR⁶; -   a compound wherein G is S(O₂), Y is methyl, R¹ is 4-carboxyphenyl,     R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is     CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is H, R¹ is     4-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is n-butyl,     R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is 4-methyl-piperazin-1-ylcarbonyl, R¹     is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵,     and R⁶ are hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is bromo, R¹ is     4-(1-hydroxyethyl)phenyl, R² is     4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are     hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is dimethylaminomethyl, R¹ is     4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A     is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is H, R¹ is 3-cyanophenyl, R² is     5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵,     and B is CR⁶; -   a compound wherein G is S, Y is methylcarbonyl, R¹ is     4-carboxyphenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are     hydrogen, A is CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is H, R¹ is 4-carboxyphenyl, R² is     2-fluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is     CR⁶; -   a compound wherein G is S, Y is H, R¹ is 4-carboxyphenyl, R² is     3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is     CR⁶; and -   a compound wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is     2-fluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is     CR⁶; -   a compound wherein G is S(O₂), Y is methyl, R¹ is 4-carboxyphenyl,     R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is     CR⁵, and B is CR⁶; -   a compound wherein G is S, Y is H, R¹ is 3-(1H-tetrazol-5-yl)phenyl,     R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are     hydrogen, A is CR⁵, and B is CR⁶;

and enantiomers, diastereomers, solvates, and pharmaceutically acceptable salts thereof.

Compounds of Formula (I) include compounds of Formula (II)

wherein Y, R¹ and R² are as defined herein; and enantiomers, diastereomers, racemates, solvates, and pharmaceutically acceptable salts thereof.

Compounds of Formula (I) include compounds of Formula (III)

wherein A, B, G, Y, and R² are as defined herein;

R^(1a) and R^(1b) are selected from the group consisting of

-   a) 2-methyl and H; -   b) 2-fluoro and hydrogen; -   c) 3-fluoro and hydrogen; -   d) 3-methyl and hydrogen; -   e) 3-fluoro and 5-fluoro; -   f) 2-fluoro and 5-fluoro; -   g) 2-chloro and hydrogen; -   h) 3-chloro and hydrogen; -   i) 2-chloro and 6-chloro; -   j) 2-trifluoromethyl and hydrogen; -   k) 3-trifluoromethyl and hydrogen; -   l) 3-trifluoromethoxy and hydrogen; and -   m) 3-cyano and hydrogen;

and enantiomers, diastereomers, solvates, and pharmaceutically acceptable salts thereof.

A further embodiment of the present invention is directed to a compound of Formula (I) selected from:

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methylethyl, c is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is adamant-1-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is hydroxymethyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-ethyl, R¹ is methyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-carboxyphenyl, R² is adamant-1-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxyethyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-carboxyphenyl, R² is cyclohexylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is hydroxymethyl, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxyethyl, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is ethyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 4-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methyl-3,4-dihydro-2H-benzo[1,4]oxazine-7-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is hydroxymethyl, R₁ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxyethyl, R₁ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-hydroxyphenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is ethyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 4-fluoro-3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is thien-2-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is acetyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is thien-2-yl, R² is 4-trifluoromethyl-3-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-[1,2,3]thiadiazol-4-yl-phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R₃, R₄, R₅, and R₆ are hydrogen, A is CR₅, and B is CR₆;

a compound of formula (I) wherein G is S, Y is hydroxymethyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is formyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is pyridin-3-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-carboxyphenyl, R² is 2-(tert-butoxy)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 3-methylphenylmethyl, R₃, R₄, R₅, and R₆ are hydrogen, A is CR₅, and B is CR₆;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 4-methoxy-3-bromophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is thien-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is pyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is thien-2-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 4-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 2-(piperidin-1-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 3-fluorophenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-oxo-2,3-dihydro-benzooxazol-6-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-ethyl, R¹ is methyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is phenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxyethyl, R¹ is ethyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is thien-3-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-hydroxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 3-hydroxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is quinolin-8-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is acetyl, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is thien-3-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ thien-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is thien-2-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 2-(morpholin-4-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is pyridin-3-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is acetyl, R¹ is methyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is hydroxymethyl, R¹ is methyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 3-methoxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 2-(tert-butoxy)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-phenoxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is dimethylamino, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 2-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-hydroxyphenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is pyridin-3-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 2-(tert-butoxy)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is hydroxymethyl, R¹ is ethyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 3-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is 2-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-fluorophenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is formyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is n-hexyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 3-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 3-phenylpropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R₁ is phenyl, R² is 2-phenylethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-fluorophenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-(tert-butoxy)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is dimethylamino, R² is 2-(tert-butoxy)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 4-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-methoxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyano, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 3-nitrophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 4-chlorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 2-(methoxycarbonyl)-2(R)-methylethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is formyl, R¹ is ethyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is pyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-carboxyphenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is quinolin-6-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is formyl, R¹ is methyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2(S)-methoxycarbonyl-2-methylethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is pyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is ethyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 5-(ethoxycarbonyl)pentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is pyrimidin-5-yl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is formyl, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 4-chlorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is methyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is hydroxymethyl, R¹ is methyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³ and R⁴ are hydrogen, R⁶ is hydrogen, A is N, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³ and R⁴ are hydrogen, R⁶ is hydrogen, A is N, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is pyridin-2-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2(R)-methoxycarbonyl-2-methylethyl R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 3-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 2-(methylsulfanyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is acetyl, R¹ is ethyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 2-(tert-butoxy)ethyl R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is quinolin-8-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 1-methyl-1H-imidazol-4-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is dimethylamino, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is formyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1-methyl-1H-imidazol-4-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is methyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is benzothiazol-6-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-methoxyethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-carboxyphenyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2,4-dimethyl-thiazol-5-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-(methoxycarbonyl)ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 2-(methoxycarbonyl)-2(S)-methylethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 2-methoxyethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is n-propyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is pyridin-3-yl, R² is quinolin-8-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxy-3-fluorophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ ethyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-nitrophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxyphenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is isoquinolin-5-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is 3-hydroxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-methoxyphenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is (N-tert-butoxy carbonylpiperidin-4-yl)methyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1,3,5-trimethyl-1H-pyrazol-4-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is acetyl, R¹ is methyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-chloropyridin-5-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is pyridin-3-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is dimethylamino, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is thien-3-yl, R² is quinolin-8-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is quinolin-6-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-phenylethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-chloropyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is thien-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 2-(phenyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-(morpholin-4-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2,4-dihydroxy-6-methyl-pyrimidin-5-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 3-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is 4-hydroxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 3-(methylcarbonyl)propyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 4-fluoro-3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is cyclohexylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 3-hydroxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-(piperidin-1-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is formyl, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is methoxycarbonylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 4-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is isoquinolin-5-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is quinolin-8-yl, R² is quinolin-8-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is formyl, R¹ is methyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is isoquinolin-5-yl, R² is quinolin-8-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1-methyl-1H-imidazol-4-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 3-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is ethyl, R² is 2-(tert-butoxy)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 3-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is acetyl, R¹ is ethyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is allyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R₁ is phenyl, R² is 2-methylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-carboxyphenyl, R² is 2-methoxyethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is n-butyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is quinolin-6-yl, R² is quinolin-8-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxyethyl, R¹ is ethyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is methoxycarbonylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2,2-difluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is pent-3-ynyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-carboxyphenyl, R² is 2-(morpholin-4-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is dimethylamino, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R₂ is 2,2-difluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is 3-methoxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is phenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is pyridin-4-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is pyridin-2-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is 3-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 3-fluorophenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is cyclohexylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-(methylsulfanyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is (N-tert-butoxy carbonylpyrroliclin-2-yl)methyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is methyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 2-(tert-butoxycarbonylamino)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 5-bromo-2-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is pyridin-3-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 2-methylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is methanesulfonylmethyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is ethyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 2-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is quinolin-8-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-bromo-5-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 2-nitrophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 2-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is ethyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 2-(morpholin-4-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxyethyl, R¹ is ethyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-carboxyphenyl, R² is 2,2-difluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 3-methylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is cyclohexylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is n-propyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 3-nitrophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, and R⁵ are hydrogen, A is CR⁵, and B is N;

a compound of formula (I) wherein G is S, Y is H, R₁ is phenyl, R² is 3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 2-phenylethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is benzo[b]thiophen-2-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 4-chlorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is 4-methoxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is (N-tert-butoxycarbonylpyrrolidin-2-yl)methyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-(methanesulfonyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 2,2-difluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxyethyl, R¹ is ethyl, R² is 2-(tert-butoxy)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-(dimethylamino)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is n-butyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is allyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶ ₆;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 2-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 1-methyl-1H-imidazol-4-yl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is N-methylpyrrolidin-2(S)-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 3-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 2-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is pyridin-2-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-(dimethylphospho)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is cyclohexyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 2-(methylsulfanyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R₁ is phenyl, R² is pyridin-3-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 4-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 2-(dimethylamino)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is methyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is ethyl, R² is 2,2-difluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is (N-tert-butoxy carbonylpyrrolidin-2-yl)methyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and Bis CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1-methyl-1H-imidazol-4-yl, R² is quinolin-8-yl methyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 2-(methanesulfonyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 2-(2-oxo-pyrrolidin-1-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 2-aminoethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is pent-3-ynyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 2-(methylsulfanyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1,2,3,4-tetrahydro-isoquinolin-8-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is dimethylamino, R² is 2,2-difluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is amino, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxyethyl, R¹ is ethyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-(2,5-dioxo-pyrrolidin-1-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is acetyl, R¹ is ethyl, R² is 2-(tert-butoxy)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is amino, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R₁ is 3-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is thien-3-yl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-methoxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 2-fluorophenyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-oxo-pyrrolidin-5(R)-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-oxo-pyrrolidin-5(S)-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶,

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-(2,2,2-trifluoro-acetyl)-1,2,3,4-tetrahydro-isoquinolin-8-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

compound of formula (I) wherein G is S, Y is acetyl, R¹ is ethyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is amino, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is 2-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 2-methoxyethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 2-(morpholin-4-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 2-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is pyridin-3-yl, R² is 3,4-difluorophenylmethyl, R³ is hydrogen, R⁴ is methoxy, R⁵ and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxyethyl, R¹ is ethyl, R² is 2-(morpholin-4-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 2-oxo-pyrrolidin-5(S)-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is acetyl, R¹ is ethyl, R² is 2-(morpholin-4-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 4-fluorophenyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-(2-oxo-pyrrolidin-1-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is 4-trifluoromethylphenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is pyridin-4-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³ is hydrogen, R⁴ is Cl, R⁵ is hydrogen, R⁶ is methoxy, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, and R⁵ are hydrogen, R⁶ is methoxy, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is benzo[b]thiophen-2-yl, R² is quinolin-8-yl methyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-trifluoromethylphenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2(R),3-dihydroxypropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, and R⁵ are hydrogen, R⁶ is methoxy, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenylmethyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is Br, R¹ is phenyl, R² is 2-(2-oxo-imidazolidin-1-yl)-ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶; or

a compound of formula (I) wherein G is S, Y is Cl, R¹ is phenyl, R² is 2-(2-oxo-imidazolidin-1-yl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is amino, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is amino, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 3-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-methylcarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is methylamino, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 2-chloropyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 6-chloro-pyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-methylcarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is dimethylamino, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is dimethylamino, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 2-chloropyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 6-chloro-pyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 2-chloropyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is pyridin-3-yl, R² is 3-fluoro-4-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is pyridin-3-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is pyridin-3-yl, R² is 3-chloro-6-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is trifluoromethyl, R¹ is phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 5-(2-methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-thien-2-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 5-methoxycarbonyl-furan-2-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1-methyl-3-trifluoromethyl-1H-pyrazol-4-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 5-(5-trifluoromethyl-isoxazol-3-yl)-thien-2-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 5-bromo-6-chloropyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 5,6-dichloropyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(pyrazol-1-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-(5-methyl-[1,3,4]oxadiazol-2-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(oxazol-5-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-ethyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-chloro-4-methylcarbonylamino-phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-chloro-imidazo[2,1-b]thiazol-5-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 6-chloro-pyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is pyridin-3-yl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-(1-hydroxy-1-methyl-ethyl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-methylcarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is pyridin-3-yl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is dimethylamino-methyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylamino-methyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is n-propylamino-methyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is pyrrolidin-1-ylmethyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is methanesulfonyl-methyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methylcarbonylphenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methylcarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-(2-methyl-pyrimidin-4-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-(2-methyl-pyrimidin-4-yl)phenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 8-methoxyquinolin-5-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 8-methoxyquinolin-5-yl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-methoxypyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-dimethylaminopyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-methoxypyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-dimethylaminopyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is methanesulfonyl-methyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is methyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is methyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is methyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is methyl, R² is 2-t-butoxyethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is methyl, R² is 3,4-difluoro-phenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is methyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is methyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 3-cyanophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(1-hydroxy-1-methyl-ethyl)phenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-pyridin-4-yloxyphenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-pyridin-3-yloxyphenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(1-hydroxy-1-methyl-ethyl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R⁴ is fluoro, R³, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R⁴ is fluoro, R³, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-methylthio-pyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-methylthiopyridin-3-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is pyridin-3-yl, R² is 3-methoxycarbonylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is pyridin-3-yl, R² is 4-methoxycarbonylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is pyrrolidin-1-ylmethyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is methyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is pyridin-3-yl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-oxo-2,3-dihydro-benzooxazol-6-yl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-carboxyphenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-bromophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-cyanophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-bromophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-methylcarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is propyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is pentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is hexyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is 3-t-butoxypropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 2-t-butoxyethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxycarbonylphenyl, R² is ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is propyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is pyridin-3-yl, R² is 3-methoxycarbonylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is pyridin-3-yl, R² is 4-methoxycarbonylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is pyridin-3-yl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is pyridin-3-yl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4,4,4-trifluoro-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-cyanophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxycarbonylphenyl, R² is 4,4,4-trifluorobutyl, R⁴ is fluoro, R³, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-aminocarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-aminocarbonylphenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxycarbonylphenyl, R² is 3-t-butoxypropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylamino-methyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is dimethylamino-methyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is formyl, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is dimethylamino-methyl, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is H, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methoxy, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methoxy, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4,4,4-trifluorobutyl, R⁴ is fluoro, R³, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R⁴ is fluoro, R³, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is H, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is bromo, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is H, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is bromo, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methoxy, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is bromo, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methoxy, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is cyclobutylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is cyclopentylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is bicyclo[2.2.1]hept-2-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is tetrahydropyran-4-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is 2-dimethylamino-ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-dimethylaminophenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-pyrrolidin-1-ylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-morpholin-4-yl-phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(1-methyl-piperazin-4-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-dimethylaminopyridin-3-yl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is n-butyl, R⁴ is fluoro, R³, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-carboxyphenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is isobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is 2-cyclohexyloxy-ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxyphenyl, R² is 3-methoxy-3-methyl-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-(2H-tetrazol-5-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-carboxyphenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is dimethylaminocarbonyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylaminocarbonyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is aminocarbonyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methylcarbonyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 3-dimethylaminosulfonylphenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 3-dimethylaminosulfonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is 1-hydroxy-1-methyl-ethyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is 1-hydroxy-ethyl, R¹ is phenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and Bis CR⁶;

a compound of formula (I) wherein G is S, Y is aminocarbonyl, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylaminocarbonyl, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is dimethylaminocarbonyl, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is aminocarbonyl, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is dimethylaminocarbonyl, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(N-hydroxy-acetamidinyl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(N-(methylcarbonyloxy)acetamidinyl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(N-hydroxy-acetamidinyl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-bromophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-carboxyphenyl, R² is cyclopropylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-carboxyphenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-carboxyphenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(N-hydroxy-acetamidinyl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is phenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 3-chloro-4-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-difluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-methanesulfonylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is pentafluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-trifluoromethylsulfonylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is pyridin-2-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 3-fluoro-4-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-nitrophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-aminophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonylamino, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyclopentyl, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyclopentyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-bromophenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-methoxycarbonylphenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-carboxyphenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-bromophenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(methanesulfonylamino)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methanesulfonylamino, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonylamino, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-carboxyethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-phenyl, R² is 4,4,4-trifluoro-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-methoxycarbonylphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 3,4,5-trifluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 2-fluoro-5-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 2,5-dichlorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-chloro-3-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-2-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is benzo[1,3]dioxol-5-ylmethyl R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;₆

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 2,2-difluoro-benzo[1,3]dioxol-5-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 3,4-dimethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-trifluoromethylthiophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxythien-2-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 5-carboxy-3-methylthien-2-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 5-carboxyfuran-2-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-methoxycarbonylphenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-methoxycarbonylphenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is methylamino, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is methylamino, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1S*-hydroxy-ethyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1R*-hydroxy-ethyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is dimethylamino, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-carboxyphenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-carboxyphenyl, R² is 5,5,5-trifluoropentyl R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-cyanophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is isopropyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is isopropyl, R¹ is phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-cyanophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-cyanophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-cyanophenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-cyanophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is methylamino, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is methylamino, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(hydroxyaminocarbonyl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-carboxyphenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R⁴ is trifluoromethyl, R³, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is n-butyl, R⁴ is trifluoromethyl, R³, R⁵, and R⁶ are hydrogen, A is CR₅, and B is CR₆;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(morpholin-4-yl)phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-dimethylaminophenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-dimethylaminophenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-morpholin-4-yl-phenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is isopropyl, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is isopropyl, R¹ is 4-methoxycarbonylphenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is isopropyl, R¹ is 4-methoxycarbonylphenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is isopropyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is isopropyl, R¹ is 4-carboxyphenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is isopropyl, R¹ is 4-carboxyphenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 3-cyanophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 3-cyanophenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 3-cyanophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 3-(1H-tetrazol-5-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is bromo, R¹ is phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 3-(1H-tetrazol-5-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-aminophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-amino-3-chloro-phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-aminophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-amino-3-bromophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxy-2-fluorophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxy-2-fluorophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxy-2-fluorophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxy-2-fluorophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxy-2-fluorophenyl, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)-phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-(methoxycarbonyl)ethyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-(methoxycarbonyl)ethyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-(methoxycarbonyl)ethyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-(methoxycarbonyl)ethyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-carboxyethyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-carboxyethyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-carboxyethyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)-phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methyl, R¹ is phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methyl, R¹ is phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methyl, R¹ is phenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methyl, R¹ is phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methyl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(methanesulfonylaminocarbonyl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(2-oxo-2,3-dihydro-2λ4-[1,2,3,5]oxathiadiazol-4-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxycarbonylphenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxycarbonylphenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxycarbonylphenyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxycarbonylphenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methyl, R¹ is 4-carboxyphenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methyl, R¹ is 4-carboxyphenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-carboxy-2-fluorophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-carboxy-2-fluorophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is dimethylamino, R¹ is phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methylamino, R¹ is phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is 4-methyl-piperazin-1-yl, R¹ is phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is amino, R¹ is phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is piperazin-1-yl, R¹ is phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is methylamino, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S(O₂), Y is 4-methyl-piperazin-1-yl, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-aminophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-amino-3-bromophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-methanesulfonylaminophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-aminophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-bromophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-bromophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-bromophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-carboxyphenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-carboxyphenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(methanesulfonylamino)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(methanesulfonylamino)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 3-bromo-4-(methanesulfonylamino)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is trifluoromethyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is trifluoromethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is trifluoromethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is trifluoromethyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-aminophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-amino-3-chloro-phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-aminophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2,2,2-trifluoroethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2,2,2-trifluoroethyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2,2,2-trifluoroethyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2,2,2-trifluoroethyl, R² is 4,4,4-trifluorobutyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2,2,2-trifluoroethyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyclopropyl, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyclopropyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(methanesulfonylamino)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(methanesulfonylamino)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-methanesulfonylaminophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(methanesulfonylamino)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(methanesulfonylamino)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 3,5-dichloro-4-(methanesulfonylamino)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 3,5-dichloro-4-(methanesulfonylamino)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 3-bromo-4-(methanesulfonylamino)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)-phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-carboxy-2-fluorophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and Bis CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-carboxy-2-fluorophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)-phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-methylaminophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-dimethylaminophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-methylaminophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 3-chloro-4-methylaminophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 3-bromo-4-methylaminophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-methylaminophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-trifluoromethylcarbonylaminophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-trifluoromethylcarbonylaminophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyclobutyl, R¹ is 4-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 2,2,2-trifluoroethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyclobutyl, R¹ is 4-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-hydroxypropyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-(2,2,2-trifluoro-acetyl)-1,2,3,4-tetrahydro-isoquinolin-7-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(2-dimethylaminomethyl-imidazol-1-yl)phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 2,2,2-trifluoroethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 2,2,2-trifluoroethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is hydroxymethyl, R¹ is 2,2,2-trifluoroethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is methylamino, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxy-2-fluorophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and Bis CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxy-2-fluorophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxy-2-fluorophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-carboxy-2-fluorophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 3-methanesulfonylaminophenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;₆

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 3-(methanesulfonylamino)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 3-(methanesulfonylamino)phenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(methanesulfonylamino)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(methanesulfonylamino)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-(cyclopropylsulfonylamino)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is 4-(cyclopropylsulfonylamino)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1H-benzimidazol-2-yl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is quinoxalin-5-yl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1-methyl-benzimidazol-2-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is quinoxalin-5-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-formylethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-hydroxy-3-methyl-butyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1H-benzimidazol-2-yl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 5-chloro-1-methyl-benzimidazol-2-yl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1H-benzimidazol-2-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1H-benzimidazol-2-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-bromophenyl, R² is 4-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-bromophenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-bromophenyl, R² is phenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-bromophenyl, R² is 3-chloro-4-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-bromophenyl, R² is 4-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-bromophenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-bromophenyl, R² is phenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-bromophenyl, R² is 3-chloro-4-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-dimethylaminophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-diethylaminophenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(thiomorpholin-4-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and Bis CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(morpholin-4-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(piperazin-1-yl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-methanesulfonylamino-2-methoxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-methanesulfonylamino-2-methoxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1-methyl-benzimidazol-2-yl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 1-methyl-benzimidazol-2-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-amino-indan-5-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-dimethylaminophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(thiomorpholin-4-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(morpholin-4-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(piperidin-1-yl)phenyl, R² is 2-(cyclopropyl)ethyl R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(piperidin-1-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyclopropyl, R¹ is 4-(methoxycarbonyl)phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyclobutyl, R¹ is 4-(methoxycarbonyl)phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyclopropyl, R¹ is 4-carboxyphenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is cyclobutyl, R¹ is 4-carboxyphenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-(methoxycarbonyl)propyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-hydroxybutyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-hydroxy-4-methylpentyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-(methoxycarbonyl)ethyl, R² is 3-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is methoxycarbonylmethyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-carboxyethyl, R² is 3-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-hydroxy-3-methyl-butyl, R² is 3-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-hydroxypropyl, R² is 3-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-carboxypropyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 5-chloro-2-methoxy-4-(methanesulfonylamino)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-methyl-1,2,3,4-tetrahydro-isoquinolin-7-yl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is isopropenyl, R¹ is ethyl, R² is 4-chloro-2-fluoro-5-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-bromopropyl, R² is 3-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is cyclopropyl, R² is 3-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-bromobutyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-cyanophenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is 4-cyanophenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and Bis CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxy-3-fluorophenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxy-3-fluorophenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is ethyl, R² is 2-fluoro-3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(4-methyl-piperazin-1-ylcarbonyl)phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-(imidazol-1-yl)propyl, R² is 3-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(imidazol-1-yl)butyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 2-hydroxy-4-(methanesulfonylamino)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is 4-carboxyphenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(pyrrolidin-3S-ylaminocarbonyl)-phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(pyrrolidin-3R-ylaminocarbonyl)-phenyl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(1H-tetrazol-5-yl)phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-dimethylamino-pyridin-3-yl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-dimethylamino-pyridin-3-yl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;₆

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-morpholin-4-yl-pyridin-3-yl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-dimethylamino-pyridin-3-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-morpholin-4-yl-pyridin-3-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is methoxycarbonylmethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is carboxymethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-hydroxyethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-methoxycarbonylethyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-carboxyethyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-hydroxy-3-methyl-butyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 2-bromoethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-morpholin-4-yl-pyridin-3-yl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-dimethylaminophenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(morpholin-4-yl)phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶; a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is ethyl, R² is 2,4,5-trifluoro-3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is isopropenyl, R¹ is ethyl, R² is 2,4,5-trifluoro-3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-(1H-tetrazol-5-yl)pyridin-3-yl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-(1H-tetrazol-5-yl)pyridin-3-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-(1H-tetrazol-5-yl)pyridin-3-yl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)pyridin-3-yl, R² is 2-(cyclopropyl)ethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-pyridin-3-yl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 6-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)pyridin-3-yl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)phenyl, R² is 4-trifluoromethoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(5-oxo-4,5-dihydro-[1,2,4]triazol-3-yl)phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-(1-methyl-5-oxo-4,5-dihydro-1H-[1,2,4]triazol-3-yl)-phenyl, R² is 5,5,5-trifluoropentyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is phenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, and R⁵ are hydrogen, A is CR⁵, and B is N;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 3-carboxyphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, and R⁵ are hydrogen, A is CR⁵, and B is N;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 4-carboxyphenyl, R² is 3,3,3-trifluoropropyl, R³, R⁴, and R⁵ are hydrogen, A is CR⁵, and B is N;

a compound of formula (I) wherein G is S, Y is chloro, R¹ is 3-methoxycarbonylphenyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, and R⁵ are hydrogen, A is CR⁵, and B is N;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 2-fluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is phenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is hydroxymethyl, R¹ is phenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-ethyl, R¹ is phenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-methoxy-ethyl, R¹ is phenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-methoxycarbonylphenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 4-carboxyphenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3,4-difluorophenyl, R² is phenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3,4-difluorophenyl, R² is 4-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-ethyl, R¹ is ethyl, R² is 4-fluoro-3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is ethyl, R² is 4-fluoro-3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 2-fluoro-pyridin-4-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is phenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3,4-difluorophenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methoxymethyl, R¹ is phenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is phenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is hydroxymethyl, R¹ is 2,5-dibromophenyl, R² is 3,4-difluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-ethyl, R¹ is ethyl, R² is 2-fluoro-pyridin-4-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is ethyl, R² is 2-fluoro-pyridin-4-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is ethyl, R² is 4-fluoro-3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-hydroxy-1-methyl-ethyl, R¹ is ethyl, R² is 4-fluoro-3-methoxyphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is 1-methoxy-ethyl, R¹ is ethyl, R² is 4-fluoro-3-trifluoromethylphenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is ethyl, R² is 2,3,5-trifluoro-pyridin-4-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3,4-difluorophenyl, R² is 2-fluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-methoxycarbonylphenyl, R² is 3-fluoropropyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is 4-methoxycarbonylphenyl, R² is 2-fluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is phenyl, R² is 2-fluoroethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-fluoro-4-(4-fluorophenylmethoxy)phenyl, R² is 4-fluorophenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methyl, R¹ is 3-fluoro-4-(phenylmethoxy)phenyl, R² is phenylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is ethyl, R² is 2-fluoro-pyridin-4-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is methylcarbonyl, R¹ is ethyl, R² is 2-fluoro-pyridin-4-ylmethyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is bromo, R¹ is n-butylamino, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

a compound of formula (I) wherein G is S, Y is H, R¹ is n-butylamino, R² is n-butyl, R³, R⁴, R⁵, and R⁶ are hydrogen, A is CR⁵, and B is CR⁶;

or a pharmaceutically acceptable salt form thereof.

A further embodiment of the present invention is directed to compounds of formula (I) wherein the compounds have a formula selected from the group consisting of

or a pharmaceutically acceptable salt form thereof.

For use in medicine, salts of compounds of formula (I) refer to non-toxic “pharmaceutically acceptable salts.” Other salts may, however, be useful in the preparation of compounds of formula (I) or of their pharmaceutically acceptable salts thereof. Suitable pharmaceutically acceptable salts of compounds of formula (I) include acid addition salts which can, for example, be formed by mixing a solution of the compound with a solution of a pharmaceutically acceptable acid such as hydrochloric acid, sulfuric acid, fumaric acid, maleic acid, succinic acid, acetic acid, benzoic acid, citric acid, tartaric acid, carbonic acid or phosphoric acid. Furthermore, where the compounds of formula (I) carry an acidic moiety, suitable pharmaceutically acceptable salts thereof may include alkali metal salts, such as sodium or potassium salts; alkaline earth metal salts, such as calcium or magnesium salts; and salts formed with suitable organic ligands, such as quaternary ammonium salts. Thus, representative pharmaceutically acceptable salts include acetate, benzenesulfonate, benzoate, bicarbonate, bisulfate, bitartrate, borate, bromide, calcium edetate, camsylate, carbonate, chloride, clavulanate, citrate, dihydrochloride, edetate, edisylate, estolate, esylate, fumarate, gluceptate, gluconate, glutamate, glycollylarsanilate, hexylresorcinate, hydrabamine, hydrobromide, hydrochloride, hydroxynaphthoate, iodide, isothionate, lactate, lactobionate, laurate, malate, maleate, mandelate, mesylate, methylbromide, methylnitrate, methylsulfate, mucate, napsylate, nitrate, N-methylglucamine ammonium salt, oleate, pamoate (embonate), palmitate, pantothenate, phosphate/diphosphate, polygalacturonate, salicylate, stearate, sulfate, subacetate, succinate, tannate, tartrate, teoclate, tosylate, triethiodide and valerate.

Representative acids and bases that may be used in the preparation of pharmaceutically acceptable salts include acids including acetic acid, 2,2-dichloroactic acid, acylated amino acids, adipic acid, alginic acid, ascorbic acid, L-aspartic acid, benzenesulfonic acid, benzoic acid, 4-acetamidobenzoic acid, (+)-camphoric acid, camphorsulfonic acid, (+)-(1S)-camphor-10-sulfonic acid, capric acid, caproic acid, caprylic acid, cinnamic acid, citric acid, cyclamic acid, dodecylsulfuric acid, ethane-1,2-disulfonic acid, ethanesulfonic acid, 2-hydroxy-ethanesulfonic acid, formic acid, fumaric acid, galactaric acid, gentisic acid, glucoheptonic acid, D-gluconic acid, D-glucoronic acid, L-glutamic acid, α-oxo-glutaric acid, glycolic acid, hippuric acid, hydrobromic acid, hydrochloric acid, (+)-L-lactic acid, (±)-DL-lactic acid, lactobionic acid, maleic acid, (−)-L-malic acid, malonic acid, (±)-DL-mandelic acid, methanesulfonic acid, naphthalene-2-sulfonic acid, naphthalene-1,5-disulfonic acid, 1-hydroxy-2-naphthoic acid, nicotinic acid, nitric acid, oleic acid, orotic acid, oxalic acid, palmitic acid, pamoic acid, phosphoric acid, L-pyroglutamic acid, salicylic acid, 4-amino-salicylic acid, sebaic acid, stearic acid, succinic acid, sulfuric acid, tannic acid, (+)-L-tartaric acid, thiocyanic acid, p-toluenesulfonic acid and undecylenic acid; and bases including ammonia, L-arginine, benethamine, benzathine, calcium hydroxide, choline, deanol, diethanolamine, diethylamine, 2-(diethylamino)-ethanol, ethanolamine, ethylenediamine, N-methyl-glucamine, hydrabamine, 1H-imidazole, L-lysine, magnesium hydroxide, 4-(2-hydroxyethyl)-morpholin, piperazine, potassium hydroxide, 1-(2-hydroxyethyl)-pyrrolidine, secondary amine, sodium hydroxide, triethanolamine, tromethamine and zinc hydroxide.

Embodiments of the present invention include prodrugs of compounds of formula (I). In general, such prodrugs will be functional derivatives of the compounds that are readily convertible in vivo into the required compound. Thus, in the methods of treating or preventing embodiments of the present invention, the term “administering” encompasses the treatment or prevention of the various diseases, conditions, syndromes and disorders described with the compound specifically disclosed or with a compound that may not be specifically disclosed, but which converts to the specified compound in vivo after administration to a patient. Conventional procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in “Design of Prodrugs”, ed. H. Bundgaard, Elsevier, 1985.

Where the compounds according to embodiments of this invention have at least one chiral center, they may accordingly exist as enantiomers. Where the compounds possess two or more chiral centers, they may additionally exist as diastereomers. It is to be understood that all such isomers and mixtures thereof are encompassed within the scope of the present invention. Furthermore, some of the crystalline forms for the compounds may exist as polymorphs and as such are intended to be included in the present invention. In addition, some of the compounds may form solvates with water (i.e., hydrates) or common organic solvents, and such solvates are also intended to be encompassed within the scope of this invention. The skilled artisan will understand that the term compound as used herein, is meant to include solvated compounds of Formula I.

Where the processes for the preparation of the compounds according to certain embodiments of the invention give rise to mixture of stereoisomers, these isomers may be separated by conventional techniques such as preparative chromatography. The compounds may be prepared in racemic form, or individual enantiomers may be prepared either by enantiospecific synthesis or by resolution. The compounds may, for example, be resolved into their component enantiomers by standard techniques, such as the formation of diastereomeric pairs by salt formation with an optically active acid, such as (−)-di-p-toluoyl-d-tartaric acid and/or (+)-di-p-toluoyl-l-tartaric acid followed by fractional crystallization and regeneration of the free base. The compounds may also be resolved by formation of diastereomeric esters or amides, followed by chromatographic separation and removal of the chiral auxiliary. Alternatively, the compounds may be resolved using a chiral HPLC column.

One embodiment of the present invention is directed to a composition, including a pharmaceutical composition, comprising, consisting of, and/or consisting essentially of the (+)-enantiomer of a compound of formula (I) wherein said composition is substantially free from the (−)-isomer of said compound. In the present context, substantially free means less than about 25%, preferably less than about 10%, more preferably less than about 5%, even more preferably less than about 2% and even more preferably less than about 1% of the (−)-isomer calculated as.

${{\%( + )} - {enantiomer}} = {\frac{\left( {{{mass}( + )} - {enantiomer}} \right)}{\left( {{{mass}( + )} - {enantiomer}} \right) + \left( {{{mass}( - )} - {enantiomer}} \right)} \times 100}$

Another embodiment of the present invention is a composition, including a pharmaceutical composition, comprising, consisting of, and consisting essentially of the (−)-enantiomer of a compound of formula (I) wherein said composition is substantially free from the (+)-isomer of said compound. In the present context, substantially free from means less than about 25%, preferably less than about 10%, more preferably less than about 5%, even more preferably less than about 2% and even more preferably less than about 1% of the (+)-isomer calculated as

${{\%( - )} - {enantiomer}} = {\frac{\left( {{{mass}( - )} - {enantiomer}} \right)}{\left( {{{mass}( + )} - {enantiomer}} \right) + \left( {{{mass}( - )} - {enantiomer}} \right)} \times 100}$

During any of the processes for preparation of the compounds of the various embodiments of the present invention, it may be necessary and/or desirable to protect sensitive or reactive groups on any of the molecules concerned. This may be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, Second Edition, J. F. W. McOmie, Plenum Press, 1973; T. W. Greene & P. G. M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991; and T. W. Greene & P. G. M. Wuts, Protective Groups in Organic Synthesis, Third Edition, John Wiley & Sons, 1999. The protecting groups may be removed at a convenient subsequent stage using methods known from the art.

Even though the compounds of embodiments of the present invention (including their pharmaceutically acceptable salts and pharmaceutically acceptable solvates) can be administered alone, they will generally be administered in admixture with a pharmaceutically acceptable carrier, a pharmaceutically acceptable excipient and/or a pharmaceutically acceptable diluent selected with regard to the intended route of administration and standard pharmaceutical or veterinary practice. Thus, particular embodiments of the present invention are directed to pharmaceutical and veterinary compositions comprising compounds of formula (I) and at least one pharmaceutically acceptable carrier, pharmaceutically acceptable excipient, and/or pharmaceutically acceptable diluent

By way of example, in the pharmaceutical compositions of embodiments of the present invention, the compounds of formula (I) may be admixed with any suitable binder(s), lubricant(s), suspending agent(s), coating agent(s), solubilizing agent(s), and combinations thereof.

Solid oral dosage forms, such as tablets or capsules, containing the compounds of the present invention may be administered in at least one dosage form at a time, as appropriate. It is also possible to administer the compounds in sustained release formulations.

Additional oral forms in which the present inventive compounds may be administered include exilirs, solutions, syrups, and suspensions; each optionally containing flavoring agents and coloring agents.

Alternatively, compounds of formula (I) can be administered by inhalation (intratracheal or intranasal) or in the form of a suppository or pessary, or they may be applied topically in the form of a lotion, solution, cream, ointment or dusting powder. For example, they can be incorporated into a cream comprising, consisting of, and/or consisting essentially of an aqueous emulsion of polyethylene glycols or liquid paraffin. They can also be incorporated, at a concentration of between about 1% and about 10% by weight of the cream, into an ointment comprising, consisting of, and/or consisting essentially of a white wax or white soft paraffin base together with any stabilizers and preservatives as may be required. An alternative means of administration includes transdermal administration by using a skin or transdermal patch.

The pharmaceutical compositions of the present invention (as well as the compounds of the present invention alone) can also be injected parenterally, for example intracavernosally, intravenously, intramuscularly, subcutaneously, intradermally or intrathecally. In this case, the compositions will also include at least one of a suitable carrier, a suitable excipient, and a suitable diluent.

For parenteral administration, the pharmaceutical compositions of the present invention are best used in the form of a sterile aqueous solution that may contain other substances, for example, enough salts and monosaccharides to make the solution isotonic with blood.

For buccal or sublingual administration, the pharmaceutical compositions of the present invention may be administered in the form of tablets or lozenges, which can be formulated in a conventional manner.

By way of further example, pharmaceutical compositions containing at least one of the compounds of formula (I) as the active ingredient can be prepared by mixing the compound(s) with a pharmaceutically acceptable carrier, a pharmaceutically acceptable diluent, and/or a pharmaceutically acceptable excipient according to conventional pharmaceutical compounding techniques. The carrier, excipient, and diluent may take a wide variety of forms depending upon the desired route of administration (e.g., oral, parenteral, etc.). Thus for liquid oral preparations, such as suspensions, syrups, elixirs and solutions, suitable carriers, excipients and diluents include water, glycols, oils, alcohols, flavoring agents, preservatives, stabilizers, coloring agents and the like; for solid oral preparations, such as powders, capsules and tablets, suitable carriers, excipients and diluents include starches, sugars, diluents, granulating agents, lubricants, binders, disintegrating agents and the like. Solid oral preparations also may be optionally coated with substances, such as, sugars, or be enterically-coated so as to modulate the major site of absorption and disintegration. For parenteral administration, the carrier, excipient and diluent will usually include sterile water, and other ingredients may be added to increase solubility and preservation of the composition. Injectable suspensions or solutions may also be prepared utilizing aqueous carriers along with appropriate additives, such as solubilizers and preservatives.

A therapeutically effective amount of a compound of formula (I) or a pharmaceutical composition thereof includes a dose range from about 0.1 mg to about 3000 mg, in particular from about 1 mg to about 1000 mg or, more particularly, from about 10 mg to about 500 mg of active ingredient in a regimen of about 1 to 4 times per day for an average (70 kg) human; although, it is apparent to one skilled in the art that the therapeutically effective amount for active compounds of the invention will vary as will the diseases, syndromes, conditions, and disorders being treated.

For oral administration, a pharmaceutical composition is preferably provided in the form of tablets containing about 0.01, about 10, about 50, about 100, about 150, about 200, about 250, and about 500 milligrams of the inventive compound as the active ingredient.

Advantageously, a compound of formula (I) may be administered in a single daily dose, or the total daily dosage may be administered in divided doses of two, three and four times daily.

Optimal dosages of a compound of formula (I) to be administered may be readily determined and will vary with the particular compound used, the mode of administration, the strength of the preparation, and the advancement of the disease, syndrome, condition, or disorder. In addition, factors associated with the particular subject being treated, including subject age, weight, diet and time of administration, will result in the need to adjust the dose to achieve an appropriate therapeutic level. The above dosages are thus exemplary of the average case. There can be, of course, individual instances wherein higher or lower dosage ranges are merited, and such are within the scope of this invention.

Compounds of formula (I) may be administered in any of the foregoing compositions and dosage regimens or by means of those compositions and dosage regimens established in the art whenever use of a compound of formula (I) is required for a subject in need thereof.

As antagonists of the TRPM8 ion channel, the compounds of formula (I) are useful in methods for treating and preventing a disease, a syndrome, a condition, or a disorder in a subject, including an animal, a mammal and a human in which the disease, the syndrome, the condition, or the disorder is affected by the modulation of TRPM8 receptors. Such methods comprise, consist of, and consist essentially of administering to a subject, including an animal, a mammal, and a human in need of such treatment or prevention a therapeutically effective amount of a compound, salt, or solvate of formula (I). In particular, the compounds of formula (I) are useful for preventing or treating pain, or diseases, syndromes, conditions, or disorders causing such pain, or pulmonary or vascular dysfunction. More particularly, the compounds of formula (I) are useful for preventing or treating inflammatory pain, inflammatory hypersensitivity conditions, neuropathic pain, anxiety, depression, and cardiovascular disease aggravated by cold, including peripheral vascular disease, vascular hypertension, pulmonary hypertension, Raynaud's disease, and coronary artery disease, by administering to a subject in need thereof a therapeutically effective amount of a compound of formula (I).

Examples of inflammatory pain include pain due to a disease, condition, syndrome, disorder, or a pain state including inflammatory bowel disease, visceral pain, migraine, post operative pain, osteoarthritis, rheumatoid arthritis, back pain, lower back pain, joint pain, abdominal pain, chest pain, labor, musculoskeletal diseases, skin diseases, toothache, pyresis, burn, sunburn, snake bite, venomous snake bite, spider bite, insect sting, neurogenic bladder, interstitial cystitis, urinary tract infection, rhinitis, contact dermatitis/hypersensitivity, itch, eczema, pharyngitis, mucositis, enteritis, irritable bowel syndrome, cholecystitis, pancreatitis, postmastectomy pain syndrome, menstrual pain, endometriosis, sinus headache, tension headache, or arachnoiditis.

One type of inflammatory pain is inflammatory hyperalgesia, which can be further distinguished as inflammatory somatic hyperalgesia or inflammatory visceral hyperalgesia. Inflammatory somatic hyperalgesia can be characterized by the presence of an inflammatory hyperalgesic state in which a hypersensitivity to thermal, mechanical and/or chemical stimuli exists. Inflammatory visceral hyperalgesia can also be characterized by the presence of an inflammatory hyperalgesic state, in which an enhanced visceral irritability exists.

Examples of inflammatory hyperalgesia include a disease, syndrome, condition, disorder, or pain state including inflammation, osteoarthritis, rheumatoid arthritis, back pain, joint pain, abdominal pain, musculoskeletal diseases, skin diseases, post operative pain, headaches, toothache, burn, sunburn, insect sting, neurogenic bladder, urinary incontinence, interstitial cystitis, urinary tract infection, cough, asthma, chronic obstructive pulmonary disease, rhinitis, contact dermatitis/hypersensitivity, itch, eczema, pharyngitis, enteritis, irritable bowel syndrome, inflammatory bowel diseases including Crohn's Disease or ulcerative colitis.

One embodiment of the present invention is directed to a method for treating inflammatory somatic hyperalgesia in which a hypersensitivity to thermal, mechanical and/or chemical stimuli exists, comprising the step of administering to a mammal in need of such treatment a therapeutically effective amount of a compound, salt or solvate of formula (I).

A further embodiment of the present invention is directed to a method for treating inflammatory visceral hyperalgesia in which a enhanced visceral irritability exists, comprising, consisting of, and/or consisting essentially of the step of administering to a subject in need of such treatment a therapeutically effective amount of a compound, salt or solvate of formula (I).

A further embodiment of the present invention is directed to a method for treating neuropathic cold allodynia in which a hypersensitivity to a cooling stimuli exists, comprising, consisting of, and/or consisting essentially of the step of administering to a subject in need of such treatment a therapeutically effective amount of a compound, salt or solvate of formula (I).

Examples of an inflammatory hypersensitivity condition include urinary incontinence, benign prostatic hypertrophy, cough, asthma, rhinitis and nasal hypersensitivity, itch, contact dermatitis and/or dermal allergy, and chronic obstructive pulmonary disease.

Examples of a neuropathic pain include pain due to a disease, syndrome, condition, disorder, or pain state including cancer, neurological disorders, spine and peripheral nerve surgery, brain tumor, traumatic brain injury (TBI), spinal cord trauma, chronic pain syndrome, fibromyalgia, chronic fatigue syndrome, neuralgias (trigeminal neuralgia, glossopharyngeal neuralgia, postherpetic neuralgia and causalgia), lupus, sarcoidosis, peripheral neuropathy, bilateral peripheral neuropathy, diabetic neuropathy, central pain, neuropathies associated with spinal cord injury, stroke, amyotrophic lateral sclerosis (ALS), Parkinson's disease, multiple sclerosis, sciatic neuritis, mandibular joint neuralgia, peripheral neuritis, polyneuritis, stump pain, phantom limb pain, bony fractures, oral neuropathic pain, Charcot's pain, complex regional pain syndrome I and II (CRPS I/II), radiculopathy, Guillain-Barre syndrome, meralgia paresthetica, burning-mouth syndrome, optic neuritis, postfebrile neuritis, migrating neuritis, segmental neuritis, Gombault's neuritis, neuronitis, cervicobrachial neuralgia, cranial neuralgia, geniculate neuralgia, glossopharyngial neuralgia, migrainous neuralgia, idiopathic neuralgia, intercostals neuralgia, mammary neuralgia, Morton's neuralgia, nasociliary neuralgia, occipital neuralgia, red neuralgia, Sluder's neuralgia, splenopalatine neuralgia, supraorbital neuralgia, vulvodynia, or vidian neuralgia.

One type of neuropathic pain is neuropathic cold allodynia, which can be characterized by the presence of a neuropathy-associated allodynic state in which a hypersensitivity to cooling stimuli exists. Examples of neuropathic cold allodynia include allodynia due to a disease, condition, syndrome, disorder or pain state including neuropathic pain (neuralgia), pain arising from spine and peripheral nerve surgery or trauma, traumatic brain injury (TBI), trigeminal neuralgia, postherpetic neuralgia, causalgia, peripheral neuropathy, diabetic neuropathy, central pain, stroke, peripheral neuritis, polyneuritis, complex regional pain syndrome I and II (CRPS I/II) and radiculopathy.

Examples of anxiety include social anxiety, post traumatic stress disorder, phobias, social phobia, special phobias, panic disorder, obsessive compulsive disorder, acute stress, disorder, separation anxiety disorder, and generalized anxiety disorder.

Examples of depression include major depression, bipolar disorder, seasonal affective disorder, post natal depression, manic depression, and bipolar depression.

GENERAL SYNTHETIC METHODS

Representative compounds of the present invention can be synthesized in accordance with the general synthetic methods described below and illustrated in the schemes that follow. Since the schemes are an illustration, the invention should not be construed as being limited by the specific chemical reactions and specific conditions described in the schemes and examples. The various starting materials used in the schemes are commercially available or may be prepared by methods well within the skill of persons versed in the art. The variables are as defined herein and within the skill of persons versed in the art.

Abbreviations used in the instant specification, particularly the schemes and examples, are as follows:

-   -   AcCl acetyl chloride     -   AcOH glacial acetic acid     -   Bn or Bzl benzyl     -   DBU 1,8-diazabicyclo[5.4.0]undec-7-ene     -   DCC dicyclohexylcarbodiimide     -   DCE 1,2-dichloroethane     -   DCM dichloromethane     -   DEAD diethyl azodicarboxylate     -   DIEA diisopropyl-ethyl amine     -   DMAP 4-(dimethylamino)pyridine     -   DMF N,N-dimethylformamide     -   DMSO dimethylsulfoxide     -   DPPA diphenylphosphoryl azide     -   EDC 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride     -   ESI electron-spray ionization     -   EtOAc ethyl acetate     -   EtOH ethanol     -   h hour     -   HATU 2-(1H-7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uranium         hexafluorophosphate methanaminium     -   HBTU O-benzotriazole-N,N,N′,N′-tetramethyl uronium         hexafluorophosphate     -   HEK human embryonic kidney     -   HPLC high performance liquid chromatography     -   LHMDS lithium bis(trimethylsilyl)amide     -   mCPBA meta-chloroperbenzoic acid     -   Me methyl     -   MeOH methanol     -   MHz megahertz     -   min minutes     -   MS mass spectroscopy     -   NaHMDS sodium bis(trimethylsilyl)amide     -   NBS N-bromosuccinimide     -   NCS N-chlorosuccinimide     -   NMR nuclear magnetic resonance     -   NT not tested     -   PCC pyridinium chlorochromate     -   Ph phenyl     -   Pd/C palladium on activated carbon     -   Pd₂(dba) [tris(dibenzylideneacetone)dipalladium(0)]     -   Ph₃P triphenylphosphine     -   PPA polyphosphoric acid     -   rt room temperature     -   TCDI 1,1′-thiocarbonyldiimidazole     -   TEA/Et₃N triethylamine     -   TFA trifluoroacetic acid     -   THF tetrahydrofuran     -   TMS tetramethylsilane     -   TMSCN trimethylsilyl cyanide

Scheme A illustrates a route for the synthesis of compounds of formula (I)-A wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; Y is hydrogen, alkyl, chloro, trifluoromethyl, C₁₋₃ alkoxy, C₃₋₆ cycloalkyl, aryl, heteroaryl, or benzo-fused heteroaryl; and R¹, R², R³, R⁴, R⁵, and R⁶ are as defined herein.

A compound of the formula A1 is either commercially available or may be prepared by known methods described in the scientific literature. A compound of the formula A1 may be converted to a compound of the formula A2 using diphenylphosphoryl azide, tert-butanol and an organic base. A compound of the formula A2 may be converted to the corresponding amine, a compound of the formula A3, by the action of HCl or another mineral acid, or by the action of an organic acid, such as trifluoroacetic acid. A compound of the formula A3 may be treated with an appropriately substituted sulfonyl chloride in the presence of a base, and optionally in the presence of an aprotic organic solvent, to afford a compound of the formula A4. A compound of the formula A4 may be treated with a base such as sodium hydride, lithium bis(trimethylsilyl)amide, n-butyllithium or potassium tert-butoxide followed by alkylation with a compound of the formula, R²X, where X is a leaving group such as bromo, chloro, iodo, tosylate, mesylate, and the like, to afford a compound of the formula (I)-A. Alternatively, a compound of the formula A4 may be treated with a triarylphosphine such as triphenylphosphine, tri-o-tolylphosphine, tri-2-furylphosphine and the like; a C₁₋₆ dialkyl azodicarboxylate such as diethyl-, diisopropyl-, or di-t-butyl-azodicarboxylate, and the like; and an appropriately substituted alcohol, R²OH, to afford a compound of the formula (I)-A.

Scheme B illustrates a route for the synthesis of compounds of formula (I)-B wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; Y is hydrogen, alkyl, or chloro; and R¹, R², R³, R⁴, R⁵, and R⁶ are as defined herein.

A compound of the formula A2 may be treated with a base such as sodium hydride, lithium bis(trimethylsilyl)amide, n-butyllithium or potassium tert-butoxide followed by alkylation with a compound of the formula, R²X, where X is a leaving group such as bromo, chloro, iodo, tosylate or mesylate, to afford a compound of the formula B1. A compound of the formula B1 may be converted to the corresponding amine, a compound of the formula B2, by the action of HCl or another mineral acid, or by the action of an organic acid, such as trifluoroacetic acid. A compound of the formula B2 may be treated with an appropriately substituted sulfonyl chloride or trifluoromethylsulfonic anhydride in the presence of a base to afford a compound of the formula (I)-B.

Scheme C illustrates a route for the synthesis of compounds of formula (I)-C wherein Y_(C) is chloro, bromo, or iodo; A and B are C(R⁵) and C(R⁶), respectively; G is S; and R¹, R², R³, R⁴, R⁵, and R⁶ are as defined herein.

A compound of the formula C1, prepared using chemistry described in scheme A may be converted to a compound of the formula C2, wherein Y_(C) is chloro, bromo or iodo, by the action of appropriate reagents. For example, treatment of a compound of the formula C1 with N-chlorosuccinimide, chlorine, or sulfuryl chloride affords a compound of the formula C2 wherein Y_(C) is chloro; similarly, treatment of a compound of the formula C1 with N-bromosuccinimide or bromine affords a compound of the formula C2 wherein Y_(C) is bromo; and treatment with N-iodosuccinimide or iodine affords a compound of the formula C2 wherein Y_(C) is iodo. A compound of the formula C2 may be treated with a base such as sodium hydride, lithium bis(trimethylsilyl)amide, n-butyllithium or potassium tert-butoxide followed by alkylation with a compound of the formula, R²X, where X is a leaving group, such as bromo, chloro, iodo, tosylate, mesylate, and the like, to afford a compound of the formula (I)-C. Alternatively, a compound of formula C2 may be treated with a triarylphosphine such as triphenylphosphine, tri-o-tolylphosphine, tri-2-furylphosphine and the like; a C₁₋₆ dialkyl azodicarboxylate such as diethyl-, diisopropyl-, and di-t-butyl-azodicarboxylate, and the like; and an appropriately substituted alcohol, R²OH, to afford a compound of the formula (I)-C.

Scheme D illustrates a route for the synthesis of compounds of formula (I)-D wherein G is S; Y_(D) is hydrogen or alkyl; and A, B, R¹, R², R³ and R⁴ are as defined herein.

A compound of the formula D1 is either commercially available or may be prepared by known methods described in the scientific literature. A compound of the formula D1, wherein X_(D) is chloro or fluoro and Y_(D) is hydrogen or alkyl, may be reacted with an R-substituted thioglycolate (wherein R is C₁₋₆alkyl) in the presence of base to afford a compound of the formula D2, which may be saponified to afford a compound of the formula D3 using conventional chemistry known to one skilled in the art. Using synthetic methods outlined in scheme A, a compound of the formula D3 may be converted to compounds of the formula (I)-D.

Scheme E illustrates a route for the synthesis of compounds of the formula (I)-E wherein Y_(E) is chloro or bromo; A is nitrogen, B is C(R⁶); G is S; and R¹, R², R³, R⁴ and R⁶ are as defined herein.

A compound of the formula E1, wherein X_(E) is a suitable leaving group such as bromo, chloro, iodo, tosylate, mesylate, or the like, is either commercially available or may be prepared by known methods described in the scientific literature. A compound of the formula E1 may be treated with a suitable oxidizing agent, such as peroxide, peracetic acid or meta-chloroperbenzoic acid, using methods known to one skilled in the art, to afford a compound of the formula E2. A compound of the formula E2 may be converted to a compound of the formula E3 using trimethylsilyl cyanide in the presence of a base. A compound of the formula E3 may be reacted with an (R_(E))-substituted thioglycolate, wherein R_(E) is C₁₋₆ alkyl, in the presence of a base to afford a compound of the formula E4. A compound of the formula E4 may be treated with sodium nitrite or potassium nitrite in the presence of copper(I) chloride and hydrogen chloride to afford a compound of the formula E5 wherein Y_(E) is chloro; or, in the presence of copper (I) bromide and hydrogen bromide to afford a compound of the formula E5 wherein Y_(E) is bromo. A compound of the formula E5 may be saponified to the corresponding carboxylic acid of a compound of the formula E6 using conventional chemistry known to one skilled in the art. Using the chemistry outlined in scheme A, a compound of the formula E6 may be converted to a compound of the formula (I)-E.

Scheme F illustrates a route for the synthesis of compounds of the formula (I)-F wherein A is nitrogen, B is C(R⁶); G is S; Y is hydrogen; and R¹, R², R³, R⁴ and R⁶ are as defined herein.

A compound of the formula F1 (wherein Y_(F) is chloro or bromo) may be prepared from a compound of the formula E6 using the synthetic methods described herein for the conversion of a compound of the formula A1 to a compound of the formula A3. A compound of the formula F1 may be converted to a compound of the formula F2 by the action of a palladium catalyst, in the presence of hydrogen gas or a source of hydrogen such as 1,3-cyclohexadiene or ammonium formate. Using the chemistry outlined in scheme A, a compound of the formula F2 may be converted to a compound of the formula (I)-F.

Scheme G illustrates a route for the synthesis of compounds of the formula (I)-G wherein Y_(G) is bromo, chloro or iodo; G is S; and A, B, R¹, R², R³ and R⁴ are as defined herein.

A compound of the formula G1 may be converted to a compound of the formula (I)-G by the action of reagents such as N-chlorosuccinimide, chlorine, or sulfuryl chloride to afford a compound of the formula (I)-G, wherein Y_(G) is chloro. Likewise, a compound of the formula (I)-G, wherein Y_(G) is bromo, may be afforded by the action of N-bromosuccinimide or bromine; and a compound of the formula (I)-G, wherein Y_(G) is iodo, may be afforded by the action of N-iodosuccinimide or iodine.

Scheme H illustrates a route for the synthesis of compounds of the formula (I)-H wherein G is S; Y is cyano and A, B, R¹, R², R³ and R⁴ are as defined herein.

A compound of the formula H1, wherein Y_(H) is bromo or iodo, may be reacted with copper(I) cyanide to afford a compound of the formula (I)-H.

Scheme I illustrates a route for the synthesis of compounds of the formula (I)-I wherein G is S; Y₁ is a substituted aryl, heteroaryl, or benzo-fused heteroaryl as defined herein; and A, B, R¹, R², R³ and R⁴ are as defined in formula (I).

A compound of the formula H1, wherein Y_(H) is bromo or iodo, may be treated with an appropriately substituted aryl-, heteroaryl-, or benzo-fused heteroaryl-boronic acid or ester; in the presence of a palladium catalyst; and a base such as cesium carbonate, sodium bicarbonate, potassium fluoride, and the like; to afford a compound of the formula (I)-I.

Scheme J illustrates a route for the synthesis of compounds of formula (I)-J wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R_(J) is C₁₋₆ alkyl, C₃₋₆ cycloalkyl, or aryl; R¹ and R² are other than a nitrogen-containing heteroaryl, and wherein R³, R⁴, R⁵, and R⁶ are as defined herein. One skilled in the art will recognize that conventional protection and deprotection steps may be required for certain chemical groups of R₁ and R₂ that are sensitive to the reaction conditions described in Scheme J.

A compound of the formula J1, prepared using chemistry described in scheme C, may be converted to a compound of the formula (I)-J by the action of an R_(J)-substituted acid chloride and a Lewis acid, such as tin(IV) chloride or aluminum(III) chloride or other reagents and methods known to one skilled in the art.

Scheme K illustrates an alternate route to compounds of the formula (I)-J, wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R_(J) is C₁₋₆ alkyl, C₃₋₆ cycloalkyl, or aryl; R¹ and R² are other than a nitrogen-containing heteroaryl; and wherein R³, R⁴, R⁵, and R⁶ are as defined herein.

A compound of the formula C1 may be treated with an R_(J)-substituted acid chloride and a Lewis acid such as tin(IV) chloride or aluminum(III) chloride, to afford a product of the formula K1. A compound of the formula K1 may be treated with a base, such as sodium hydride, lithium bis(trimethylsilyl)amide, n-butyllithium or potassium tert-butoxide, followed by alkylation with a compound of the formula R²X, defined herein, to afford a compound of the formula (I)-J. Alternatively, a compound of formula K1 may be treated with a triarylphosphine such as triphenylphosphine, tri-o-tolylphosphine, tri-2-furylphosphine and the like; a C₁₋₆ dialkyl azodicarboxylate such as diethyl-, diisopropyl-, or di-t-butyl-azodicarboxylate, and the like; and an appropriately substituted alcohol, R²OH, to afford a compound of the formula (I)-J.

Scheme L illustrates a route for the synthesis of compounds of the formula (I)-L wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R¹ and R² are other than a nitrogen-containing heteroaryl; and R³, R⁴, R⁵, and R⁶ are as defined herein. One skilled in the art will recognize that conventional protection and deprotection steps may be required for certain chemical groups of R₁ and R₂ that are sensitive to the reaction conditions described in Scheme L.

A compound of the formula J1 may be treated with dichloromethyl methyl ether and a Lewis acid such as titanium(IV) chloride, to afford a compound of the formula L1. A compound of the formula L1 may be converted to a compound of the formula (I)-L using a reducing agent such as borane, sodium borohydride, lithium borohydride, and the like, to effect reduction of an aldehyde to an alcohol.

Scheme M illustrates a route for the synthesis of compounds of the formula (I)-M wherein R_(M) is C₁₋₅alkyl or C₆₋₁₀aryl; A and B are C(R⁵) and C(R⁶), respectively; G is S; R¹ and R² are other than a nitrogen-containing heteroaryl; and R³, R⁴, R⁵, and R⁶ are as defined herein. One skilled in the art will recognize that conventional protection and deprotection steps may be required for certain chemical groups of R¹ and R² that are sensitive to the reaction conditions described in Scheme M.

A compound of the formula L1 may be treated with a metal-alkyl compound, such as C₁₋₅alkylmagnesium bromide, C₁₋₅alkylzinc chloride or C₁₋₅alkyllithium, to afford a compound of the formula (I)-M wherein R_(M) is C₁₋₅alkyl. Similarly, a compound of the formula L1 may be treated with an metal-aryl compound, such as C₆₋₁₀arylmagnesium bromide, C₆₋₁₀arylzinc chloride or C₆₋₁₀aryllithium, to afford a compound of the formula (I)-M wherein R_(M) is C₆₋₁₀aryl.

Scheme N illustrates an alternate route to the compounds of the formula (I)-M wherein R_(M) is C₁₋₅alkyl. In formula (I)-N, A and B are C(R⁵) and C(R⁶), respectively; G is S; R¹ and R² are other than a nitrogen-containing heteroaryl; and R³, R⁴, R⁵, and R⁶ are as defined herein. One skilled in the art will recognize that conventional protection and deprotection steps may be required for certain chemical groups of R₁ and R₂ that are sensitive to the reaction conditions described in Scheme N.

A compound of the formula N1 may be converted to a compound of the formula (I)-N using reagents such as borane, sodium borohydride, lithium borohydride, and the like, to effect reduction of a ketone to an alcohol.

Scheme O illustrates a route for the synthesis of compounds of the formula (I)-O wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R¹ and R² are other than a nitrogen-containing heteroaryl; and R³, R⁴, R⁵, and R⁶ are as defined herein. One skilled in the art will recognize that added conventional protection and deprotection steps may be required for certain chemical groups of R¹ and R² that are sensitive to the reaction conditions described in Scheme O.

A compound of the formula O1 may be treated with a metal-C₁₋₃alkyl compound, such as C₁₋₃alkylmagnesium bromide, C₁₋₃alkylzinc chloride or C₁₋₃alkyllithium, to afford a compound of the formula (I)-O.

Scheme P illustrates a route for the synthesis of compounds of formula (I)-P wherein G is S; and Y, A, B, R², R³ and R⁴ are as defined herein.

A compound of the formula P1 (wherein Rp is C₁₋₄ alkyl) may be prepared using chemistry described in scheme A. A compound of the formula P1 may be converted to a compound of the formula (I)-P by the action of agents such as hydroxide, hydrochloric acid, trimethylsilyl iodide, or other reagents and conditions known to one skilled in the art, to effect the conversion of esters to carboxylic acids.

Scheme Q illustrates a route for the synthesis of compounds of the formula (I)-Q and formula (I)-Q1 wherein Y_(Q) is hydrogen, C₁₋₆ alkyl, or chloro; G is S; and A, B, R², R³ and R⁴ are as defined herein.

Chlorosulfonyl isocyanate, compound Q1, may be treated with tert-butanol to afford compound Q2, which may be reacted with a compound of the formula Q3 to afford a compound of the formula Q4. A compound of the formula Q4 may be converted to the corresponding amine, a compound of the formula (I)-Q, by the action of HCl or another mineral acid, or by the action of an organic acid, such as trifluoroacetic acid. Alkylation of a compound of the formula Q4 using a conventional alkylating agent such as C₁₋₆alkyl halide or C₁₋₆alkyl tosylate, in the presence of a base such as sodium hydride, affords a compound of the formula Q5 which, upon amino deprotection, affords a compound of the formula (I)-Q1.

Scheme R illustrates a route for the synthesis of compounds of the formula (I)-R and formula (I)-R¹ wherein Y_(R) is chloro, bromo or iodo; G is S; R¹ is amino or C₁₋₆ alkylamino, respectively; and A, B, R², R³ and R⁴ are as defined herein.

A compound of the formula R1 may be converted to a compound of the formula R2, wherein Y_(R) is chloro, bromo or iodo, using chemistry described in scheme C for the conversion of a compound of the formula C1 to a compound of the formula C2. A compound of the formula R2 may be converted to a compound of the formula (I)-R, using chemistry described in scheme Q for the conversion of a compound of the formula Q4 to a compound of the formula (I)-Q. A compound of the formula R² may be alkylated using conventional alkylating agents and condition such as a C₁₋₆alkyl halide in the presence of TEA or pyridine to afford a compound of the formula R³. Subsequent removal of the amino protecting group as described herein affords a compound of the formula (I)-R1.

Scheme S illustrates a route for the synthesis of compounds of formula (I)-S wherein Y_(s2) is C₁₋₃dialkylamino, or a 5 or 6 membered heterocycle with 1 to 2 nitrogens, wherein the point of attachment is via a nitrogen atom; G is S; and A, B, R¹, R², R³ and R⁴ are as defined herein.

A compound of the formula S1 wherein Y_(si) is bromo or iodo, may be converted to a compound of the formula (I)-S by the action of an appropriately substituted amine, in the presence of a palladium catalyst and a base.

Scheme T illustrates a route for the synthesis of compounds of formula (I)-T, wherein W is O or S; G is S; and A, B, Y, R², R³ and R⁴ are as defined herein.

A compound of the formula T1 may be treated with hydroxylamine hydrochloride, in the presence of a tertiary base such as triethylamine, to afford a compound of the formula T2. A compound of the formula T2 may be converted to a compound of the formula (I)-T by the reaction of either 1,1′-thiocarbonyldiimidazole (W═S) or 1,1′-carbonyldiimidazole (W═O).

Scheme U illustrates a route for the synthesis of compounds of formula (I)-U wherein G is S; and A, B, Y, R², R³, and R⁴ are as defined herein.

A compound of the formula T2 may be treated with thionyl chloride, in the presence of a non-nucleophilic base, such as pyridine, to afford a compound of the formula (I)-U.

Scheme V illustrates a route for the synthesis of compounds of the formula (I)-V wherein G is S; and A, B, Y, R², R³, and R⁴ are as defined herein.

A compound of the formula T2 may be treated with a base, such as sodium hydride, in the presence of carbon disulfide, to afford a compound of the formula (I)-V.

Scheme W illustrates a route for the synthesis of compounds of the formula (I)-W wherein G is S; and A, B, Y, R², R³, R⁴, R¹³, and R¹⁴ are as defined herein.

A compound of the formula T1, may be converted to a compound of the formula W1 wherein R_(W) is methyl or ethyl, by treatment of a compound of the formula T1 with an alcohol, such as methanol or ethanol, in the presence of hydrochloric acid. A compound of the formula W1 may be treated with a base, such as triethylamine, in the presence of a R¹³-substituted acid chloride, to afford a compound of the formula W2. Treatment of a compound of the formula W2 with a R¹⁴-substituted hydrazine, may afford a compound of the formula (I)-W.

Scheme X illustrates a route for the synthesis of compounds of the formula (I)-X wherein G is S; and A, B, Y, R², R³, R⁴, and R¹³ are as defined herein.

A compound of the formula W2 may be treated with a base, such as sodium methoxide, and in the presence of hydroxylamine hydrochloride, to afford a compound of the formula (I)-X.

Scheme Y illustrates a route for the synthesis of compounds of the formula (I)-Y wherein G is S; and A, B, Y, R², R³, R⁴, and R¹⁴ are as defined herein.

A compound of the formula W1 may be treated with 2,4,6-trimethylpyridine, in the presence of methyl chloroformate, to afford a compound of the formula Y1. Treatment of a compound of the formula Y1 with a R¹⁴-substituted hydrazine, may afford a compound of the formula (I)-Y.

Scheme Z illustrates a route for the synthesis of compounds of the formula (I)-Z wherein R³ is a substituent as defined herein other than bromo; G is S; and A, B, R¹, R², and R⁴ are as defined herein.

A compound of the formula Z1 may be prepared according to the chemistry described in scheme A. A compound of the formula Z1, wherein Y_(z) is bromo or iodo, may be reacted with an C₁₋₄ alkyllithium, followed by treatment with an electrophilic fluorinating reagent such as FClO₃ or N-fluorobenzenesulfonamide, to afford a compound of the formula (I)-Z.

Scheme AA illustrates a route for the synthesis of compounds of the formula (I)-AA wherein G is S; and A, B, Y, R², R³, and R⁴ are as defined herein.

A compound of the formula T1 may be treated with sodium azide, in the presence of a ammonium chloride or triethylamine hydrochloride, to afford a compound of the formula (I)-AA.

Scheme BB illustrates a route for the synthesis of compounds of the formula (I)-BB wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; Y is C₁₋₂ alkyl substituted with NR⁷R⁸; and R¹, R², R³ and R⁴ are as defined herein.

A compound of the formula BB1 (R_(BB) is hydrogen or methyl) may be reacted with an amine of the formula NHR⁷R⁸ (wherein R⁷ is other than C₁₋₃alkylcarbonyl and C₁₋₃ alkylsulfonyl and R⁸ is C₁₋₄ alkyl) in the presence of a hydride source such as sodium borohydride, sodium triacetoxyborohydride, and the like, in an organic solvent to afford a compound of the formula (I)-BB. A compound of the formula (I)-BB wherein R² is hydrogen may be treated in the presence of a base, optionally in the presence of an organic solvent, with an appropriately substituted acylating agent such as a C₁₋₃allyl acid chloride, or with an appropriately substituted sulfonylating agent, to afford a corresponding compound of the present invention wherein R² is C₁₋₃ alkylcarbonyl or C₁₋₃alkylsulfonyl, respectively.

Scheme CC illustrates a route for the synthesis of intermediates of the formula CC6 wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; Y_(CC) is C₁₋₆allyl; and R¹, R², R³ and R⁴ are as defined herein.

A compound of the formula CC1 is either commercially available or may be prepared by known methods such as those described in the scientific literature. A compound of the formula CC1 may be converted to a methyl bromide of the formula CC2 by the action of bromine in methanol. The bromide of a compound of the formula CC2 may undergo a nucleophilic displacement with an appropriately substituted thiol, in the presence of a base, to afford a compound of the formula CC3, which may subsequently be cyclized in the presence of PPA, optionally in an organic solvent such as chlorobenzene, to afford a compound of the formula CC4. Deprotonation with an organometallic base such as n-butyllithium followed by the addition of DMF affords an aldehyde of the formula CC5. The aldehyde group may be oxidized in the presence of a strong oxidizing agent such as potassium permanganate to afford a carboxylic acid of the formula CC6, which may be converted to a compound of the general formula (I) by the synthetic methods outlined in scheme A.

Scheme DD illustrates a route for the synthesis of compounds of the formula (I)-DD wherein A and B are C(R⁵) and C(R⁶), respectively; G is S(O₂); R¹ is other than an C₁₋₃ alkylthio-substituted substituent; and Y, R², R³ and R⁴ are as defined herein.

A compound of the formula DD1 may be prepared by the synthetic methods described herein. A compound of the formula DD1 may be treated with and oxidizing agent such as mCPBA, oxone, peracetic acid, and the like, in an organic solvent such as chloroform to afford a compound of the formula (I)-DD.

Scheme EE illustrates a route for the synthesis of compounds of the formula (I)-EE wherein A and B are C(R⁵) and C(R⁶), respectively; G is S(O₂); Y is C₁₋₃ alkoxy; and R¹, R², R³ and R⁴ are as defined herein.

A compound of the formula EE1 wherein Y_(EE) is chloro, bromo, or iodo, may be treated with a strong non-nucleophilic base such as sodium hydride, a lower alkoxide, sodium hydroxide or potassium hydroxide, DBU, and the like; in the presence of a C₁₋₃alcoholic solvent; to afford the corresponding compound of the formula (I)-EE wherein Y is a C₁₋₃alkoxy group.

Scheme FF illustrates a route for the synthesis of compounds of the formula (I)-FF wherein A and B are C(R⁵) and C(R⁶), respectively; G is S(O₂); Y is NR⁹R¹⁰; R¹ is other than C₁₋₆ alkyl substituted with bromo; and R², R³ and R⁴ are as defined herein.

A compound of the formula EE1 may be treated with an appropriately substituted amine of the formula NHR⁹R¹⁰ (wherein R⁹ is other than C₁₋₃alkylcarbonyl and C₁₋₃ alkylsulfonyl and R¹⁰ is C₁₋₄ alkyl) in an aprotic organic solvent to afford a compound of the formula (I)-FF. A compound of the formula (I)-FF wherein R⁹ is hydrogen may be treated in the presence of a base, optionally in the presence of an organic solvent, with an appropriately substituted acylating agent such as a C₁₋₃alkyl acid chloride, or with an appropriately substituted sulfonylating agent, to afford a corresponding compound of the present invention wherein R⁹ is C₁₋₃ alkylcarbonyl or C₁₋₃ alkylsulfonyl, respectively.

Scheme GG illustrates a route for the synthesis of compounds of the formula (I)-GG wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R¹ and R² are other than a nitrogen containing heteroaryl; R_(G) and R_(G1) are independently hydrogen or methyl such that Y is aminocarbonyl, methylaminocarbonyl, or dimethylaminocarbonyl; and R³ and R⁴ are as defined herein.

A compound of the formula L1 wherein Y is formyl may be converted to a carboxylic acid of the formula GG1 by the action of an oxidizing agent such as potassium permanganate. Treatment of a compound of the formula GG1 with an amine of the formula NHR_(G)R_(G1) in the presence of a coupling agent such as HBTU, DCC, HATU, and the like; and a tertiary amine such as diisopropylethylamine; in an aprotic solvent, affords an amide of the formula (I)-GG.

Scheme HH illustrates a route for the synthesis of compounds of the formula (I)-HH wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; Y is NR⁹R¹⁰, R⁹ is C₁₋₃ alkylcarbonyl or C₁₋₃ alkylsulfonyl, and R¹⁰ is hydrogen.

A compound of the formula GG1 may be treated with DPPA and tBuOH in the presence of a tertiary amine such as DIEA to afford a t-butyl carbamate of the formula HH1. Upon treatment with a mineral acid such as HCl in dioxane, the corresponding amine of the formula HH2 may be prepared. The amino group of a compound of the formula HH2 may be acylated with a C₁₋₃alkyl-substituted acid chloride or anhydride to afford a compound of the formula (I)-HH. Further treatment with a conventional C₁₋₃ alkylating agent may provide compounds of the present invention wherein R¹⁰ is C₁₋₃alkyl. Likewise, a compound of the formula HH2 may be treated with an appropriately substituted sulfonylating agent to afford a corresponding compound of the present invention wherein R⁹ is C₁₋₃alkylsulfonyl, respectively.

Scheme II illustrates a route for the synthesis of compounds of the formula (I)-II wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R¹ is CF₃; and Y, R², R³ and R⁴ are as defined herein.

A compound of the formula II1 may be converted to a compound of the formula II2 by the action of trifluoromethanesulfonic anhydride and a tertiary amine followed by treatment with hydroxide. A compound of the formula II2 may be treated with a base such as sodium hydride, lithium bis(trimethylsilyl)amide, n-butyllithium or potassium tert-butoxide followed by alkylation with a compound of the formula, R²X, where X is a leaving group such as bromo, chloro, iodo, tosylate, mesylate, and the like, to afford a compound of the formula (I)-II. Alternatively, a compound of the formula II2 may be treated with a triarylphosphine such as triphenylphosphine, tri-o-tolylphosphine, tri-2-furylphosphine and the like; a C₁₋₆ dialkyl azodicarboxylate such as diethyl-, diisopropyl-, or di-t-butyl-azodicarboxylate, and the like; and an appropriately substituted alcohol, R²OH, to afford a compound of the formula (I)-II.

Scheme JJ illustrates a route for the synthesis of compounds of the formula (I)-JJ wherein R¹ is C₁₋₆ alkyl substituted with hydroxy; formula (I)-JJ1 wherein R¹ is C₁₋₆ alkyl substituted with bromo; and formula (I)-JJ2 wherein R¹ is unsubstituted C₃₋₈ cycloalkyl; A and B are C(R⁵) and C(R⁶), respectively; and G, Y, R², R³ and R⁴ are as defined herein.

A compound of the formula JJ1 (wherein R is C₁₋₄ alkyl) may be prepared according to the synthetic methods outlined in scheme A using an appropriately substituted alkylating agent of the formula R²X or R²OH. A compound of the formula JJ1 may be converted to its corresponding alcohol of the formula (I)-JJ by the action of a reducing agent such as lithium aluminum hydride, lithium borohydride, and the like. The alcohol of the formula (I)-JJ may be treated with a brominating agent such as thionyl bromide; phosphorus tribromide; carbon tetrabromide in the presence of a triarylphosphine such as triphenylphosphine, tri-o-tolylphosphine, tri-2-furylphosphine; and the like, to afford a bromide of the formula (I)-JJ1 wherein R¹ is C₁₋₆ alkyl substituted with bromo. Treatment with a base such as sodium imidazolide, DBU, potassium tert-butoxide, and LDA, affords a cyclized product of the formula (I)-JJ2 wherein R¹ is unsubstituted C₃₋₈ cycloalkyl.

Scheme KK illustrates a route for the synthesis of compounds of the formula (I)-JJ wherein R¹ is C₁₋₆ alkyl substituted with a heteroaryl as defined herein, wherein the point of attachment is a nitrogen atom; A and B are C(R⁵) and C(R⁶), respectively; and G, Y, R², R³ and R⁴ are as defined herein.

A bromide of the formula (I)-JJ1 may be displaced by a 5 to 6 membered NH-containing heteroaryl (HET) in an organic solvent to afford a compound of the formula (I)-KK.

Scheme LL illustrates a route for the synthesis of compounds of the formula (I)-LL wherein R¹ is phenyl substituted with C(O)NHOH; and G, A, B, Y, R², R³ and R⁴ are as defined herein. One skilled in the art will recognize that added protection and deprotection steps may be required for certain chemical groups of Y that are sensitive to the reaction conditions described in Scheme LL.

A compound of the formula LL1 may be treated with O-benzyl-hydroxylamine in the presence of a coupling agent such as EDC, HATU, HBTU, and the like to afford a compound of the formula LL2. Removal of the benzyl group by the action of boron tribromide or TFA in an organic solvent such as DCM; or with a palladium catalyst in the presence of a hydrogen source such as hydrogen gas; affords a compound of the formula (I)-LL.

Scheme MM illustrates a route for the synthesis of compounds of the formula (I)-MM wherein R¹ is heteroaryl; and formula (I)-MM1 wherein R¹ is a benzo-fused heteroaryl substituted at a nitrogen atom within the ring with C₁₋₃ alkyl; G is S; and Y, A, B, R², R³ and R⁴ are as defined herein.

A compound of the formula MM1 is either commercially available or may be prepared by known methods such as those described in the scientific literature. A compound of the formula MM1 may be converted to a useful intermediate of the formula MM2 by the action of aqueous acetic acid and chlorine gas. A compound of the formula MM3 may be sulfonylated with a sulfonyl chloride of the formula MM2 to afford a compound of the formula MM4. The R² group of the present invention may be installed as previously described herein to afford a compound of the formula (I)-MM. Treatment of a compound of the formula (I)-MM with a base such as DBU in the presence of an alkylating agent such as a C₁₋₃ alkyl halide or dimethylsulfate in DMF affords a methylated compound of the formula (I)-MM1 of the present invention.

Scheme NN illustrates a route for the synthesis of compounds of the formula (I)-NN wherein G is S; Y_(NN) is bromo, chloro, iodo; and A, B, R², R³, and R⁴ are as defined herein.

A compound of the formula (I)-U may be treated with N-chlorosuccinimide or chlorine to afford a compound of the formula (I)-NN, wherein Y_(NN) is chloro. Likewise, a compound of the formula (I)-NN wherein Y_(NN) is bromo may be afforded by the action of N-bromosuccinimide or bromine; and a compound of the formula (I)-NN wherein Y_(NN) is iodo may be afforded by the action of N-iodosuccinimide or iodine.

Scheme OO illustrates a route for the synthesis of compounds of the formula (I)-OO wherein G is S; R¹ is a ring selected from phenyl or pyridin-3-yl, wherein said ring is substituted with NR¹⁵R¹⁶ wherein NR¹⁵R¹⁶ is other than NH₂; and A, B, Y, R², R³, and R⁴ are as defined herein.

A compound of the formula OO1 (wherein X_(oo) is a reactive leaving group such as fluoro, chloro, or bromo) may be prepared according to the synthetic methods described herein. A compound of the formula OO1 may be treated with a cyclic or acyclic amine of the formula HNR¹⁵R¹⁶ under basic conditions, in the presence of a palladium catalyst such as Pd₂(dba) and an appropriate ligand such as 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene, to afford a compound of the formula (I)-OO.

Scheme PP illustrates a route for the synthesis of compounds of the formula (I)-PP wherein G is S; R¹ is phenyl substituted with C(O)NR¹⁷R¹⁸ wherein R¹⁷ is C₁₋₃ alkylsulfonyl and R¹⁸ is hydrogen; and A, B, Y, R², R³, and R⁴ are as defined herein.

One skilled in the art will recognize that added protection and deprotection steps may be required for certain chemical groups of Y that are sensitive to the reaction conditions described in Scheme PP.

A compound of the formula (I)-P may be treated with the coupling agent CDI, followed by the addition of a C₁₋₃alkylsulfonamide in the presence of DBU and dimethylaminopyridine to afford a compound of the formula (I)-PP.

Scheme QQ illustrates a route for the synthesis of compounds of the formula (I)-QQ wherein G is S; R¹ is a ring selected from indanyl or tetralinyl, wherein said ring is attached via an unsaturated carbon atom and the unsaturated portion of the ring is substituted with an amino, alkylamino, or dialkylamino group; and A, B, Y, R², R³, and R⁴ are as defined herein.

A compound of the formula QQ1 is either commercially available or may be prepared by known methods such as those described in the scientific literature. A compound of the formula QQ1 may be treated with phthalic anhydride to afford a compound of the formula QQ2, which may be converted to a compound of the formula QQ3 by the action of DMF and DMAP. A compound of the formula QQ3 may be treated with chlorosulfonic acid to afford a compound of the formula QQ4. A compound of the formula III may be sulfonylated with a compound of the formula QQ4 in the presence of an aprotic organic base, such as pyridine, to afford a compound of the formula QQ5. A compound of the formula QQ5 may be alkylated as described herein to install the R² group and form a compound of the formula QQ6. Treatment of the phthalimido group of a compound of the formula QQ6 with hydrazine in methanol affords a compound of the formula (I)-QQ.

Scheme RR illustrates a route for the synthesis of compounds of the formula (I)-RR wherein G is S; R¹ is phenyl substituted with C(O)NR¹⁷R¹⁸; and A, B, Y, R², R³, and R⁴ are as defined herein.

One skilled in the art will recognize that added protection and deprotection steps may be required for certain chemical groups of Y that are sensitive to the reaction conditions described in Scheme RR.

A compound of the formula (I)-P may be coupled with an amine of the formula HNR¹⁷R¹⁸, wherein R¹⁷ and R¹⁸ are as defined herein, in the presence of a coupling agent such as HATU, DCC, and the like, and a tertiary amine such as DIEA, to afford a compound of the formula (I)-RR.

Scheme SS illustrates a route for the synthesis of compounds of the formula (I)-SS wherein G is S; Y is isopropenyl; and A, B, R¹, R², R³, and R⁴ are as defined herein.

A compound of the formula SS1 may be treated with an solution of a mineral acid such as HCl, or an organic acid such as trifluoroacetic acid, to afford a dehydrated compound of the formula (I)-SS.

Scheme TT illustrates a route for the synthesis of compounds of the formula (I)-TT wherein Y is other than bromo or iodo; R¹ is phenyl substituted with carboxy; R² is other than an aromatic bromide; and A, B, G, R³, and R⁴ are as defined herein.

A compound of the formula TT1 may be prepared using the synthetic methods outlined herein. A compound of the formula TT1 may be sulfonylated with a bromo-substituted phenylsulfonyl chloride of the formula TT2 in the presence of a base such as pyridine or DIEA to afford a compound of the formula TT3. A compound of the formula TT3 may be converted to its corresponding ester of the formula TT4 by the action of carbon monoxide in the presence of a palladium catalyst and an alcoholic solvent, such as methanol. A compound of the formula TT4 may be alkylated with an appropriate R²-substituted alkylating agent as described herein to afford a compound of the formula TT5 which, upon saponification with hydroxide, affords a carboxylic acid of the formula (I)-TT.

Scheme UU illustrates a route for the synthesis of compounds of the formula (I)-UU wherein R¹ is phenyl substituted at the 3- or 4-position with imidazolyl substituted with an aminomethyl, methylamino-methyl, or dimethylamino-methyl substitutent; R_(U) and R_(U1) are independently hydrogen or methyl; and A, B, G, Y, R², R³, and R⁴ are as defined herein.

A compound of the formula UU1 is either commercially available or may be prepared by known methods such as those described in the scientific literature. A compound of the formula UU1 may be treated with an amine of the formula NHR_(U)R_(U1) in the presence of a hydride source such as sodium borohydride, sodiumtriacetoxyborohydride, and the like, in an alcoholic solvent such as methanol to afford a compound of the formula UU2. A 3- or 4-iodo substituted compound of the formula UU3 may be prepared by the synthetic methods outlined herein. A compound of the formula UU3 may be coupled with a compound of the formula UU2 in the presence of a catalyst such as copper iodide in an organic solvent such as DMSO and a base such as K₂CO₃ to afford a compound of the formula (I)-UU.

Scheme VV illustrates a route for the synthesis of compounds of the formula (I)-VV wherein R¹ is phenyl substituted with NR¹⁵R¹⁶ wherein R¹⁵ is hydrogen or C₁₋₃alkylsulfonyl; and R¹⁶ is as defined; and A, B, G, R², R³, and R⁴ are as defined herein.

A compound of the formula VV1 is either commercially available or may be prepared by known methods such as those described in the scientific literature. The reduction of the nitro group of a compound of the formula VV1 may be achieved by a number of conventional methods, such as in the presence of a palladium catalyst under a hydrogen gas atmosphere in an alcoholic solvent such as methanol; or, by the action of iron metal in the presence of a suitable acidic reagent or solvent such as hydrochloric acid or acetic acid; or by using zinc and ammonium chloride in methanol and water; to afford the corresponding aniline of the formula (I)-V. A compound of the formula (I)-V may be sulfonylated using an appropriately substituted sulfonyl chloride in the presence of a base such as pyridine, DIEA, and the like to afford a compound of the formula (I)-V1. Compounds of the formulae (I)-V and (I)-V1 may be alkylated using conventional C₁₋₃alkylating agents to afford compounds of the invention wherein R¹⁶ is an alkyl group.

Scheme WW illustrates a route for the synthesis of compounds of the formula (I)-WW wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R^(x) and R^(y) are both hydrogen or taken together with the carbon atom to which they are both attached to form a cyclopropyl ring; Q is a bond; m is 0 or 1; and Y, R², R³ and R⁴ are as defined herein.

A compound of the formula WW1 is either commercially available or may be prepared by known methods such as those described in the scientific literature. A compound of the formula WW1 may be converted to a compound of the formula WW2 using chlorosulfonic acid, with or without organic solvent. A compound of the formula II1 may be sulfonylated with a sulfonyl chloride of the formula WW2 to afford a compound of the formula WW3. A compound of formula WW3 may be converted to a methyl ester by treatment with a reagent such as diazomethane, concentrated sulfuric acid in methanol, and the like, to afford a compound of the formula WW4. The R² group of the present invention may be installed as previously described herein to afford a compound of the formula WW5. A compound of the formula WW5 may be converted to the corresponding carboxylic acid, a compound of the formula (I)-WW, by the action of agents such as hydroxide, hydrochloric acid, trimethylsilyl iodide, or other reagents and conditions known to one skilled in the art, to effect the conversion of esters to carboxylic acids.

Scheme XX illustrates a route for the synthesis of compounds of the formula (I)-XX wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R^(x)R^(y) are each methyl; Q is a bond; m is 0 or 1; and Y, R², R³ and R⁴ are as defined herein.

A compound of the formula XX1 is either commercially available or may be prepared by known methods such as those described in the scientific literature. A compound of the formula XX1 may be converted to a compound of the formula XX2 by treatment with a reagent such as diazomethane, concentrated sulfuric acid in methanol, and the like, to afford a compound of the formula XX2. A compound of the formula XX2 may be converted to a compound of the formula XX3 using chlorosulfonic acid, with or without organic solvent. A compound of the formula II1 may be sulfonylated with a sulfonyl chloride of the formula XX3 to afford a compound of the formula XX4. The R² group of the present invention may be installed as previously described herein to afford a compound of the formula XX5. A compound of the formula XX5 may be converted to the corresponding carboxylic acid, a compound of the formula (I)-XX, by the action of agents such as hydroxide, hydrochloric acid, trimethylsilyl iodide, or other reagents and conditions known to one skilled in the art, to effect the conversion of esters to carboxylic acids.

Scheme YY illustrates a route for the synthesis of compounds of the formula (I)-YY wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R^(x) and R^(y) are independently selected from hydrogen or methyl; or R^(x) and R^(y) are taken together with the carbon atom to which they are both attached to form a cyclopropyl ring; Q is oxygen; m is 0 or 1; and Y, R², R³ and R⁴ are as defined herein.

A compound of the formula YY1 of the present invention may be prepared as previously described herein. A compound of the formula YY1 may be converted to a compound of the formula YY2 by treatment with boron tribromide in dichloromethane. A compound of the formula YY2 may be alkylated with an alkylating agent such as methyl bromoacetate, methyl 2-bromoisobutyrate, and the like, in the presence of a base, such as cesium carbonate or potassium carbonate, in a solvent such as DMF, THF, or DMSO to afford a compound of the formula YY3. A compound of the formula YY3 may be converted to the corresponding carboxylic acid, a compound of the formula (I)-YY, by the action of reagents such as hydroxide, hydrochloric acid, trimethylsilyl iodide, or other reagents and conditions known to one skilled in the art, to effect the conversion of esters to carboxylic acids.

Scheme ZZ illustrates a route for the synthesis of compounds of the formula (I)-ZZ wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; and Y, R², R³ and R⁴ are as defined herein.

A compound of the formula ZZ1 of the present invention may be prepared as previously described herein. A compound of the formula ZZ1 may be treated with a base, such as n-butyllithium, and sulfur dioxide, followed by treatment with n-chlorosuccinimide, in a solvent such as THF, to afford a compound of formula ZZ2. A compound of formula ZZ2 may be converted to a protected sulfonamide of the formula ZZ3 by treatment with tert-butyl amine. Amino deprotection of a compound of the formula ZZ3 using conventional chemistry known to one skilled in the art provides a compound of formula (I)-ZZ.

Scheme AAA illustrates a route for the synthesis of compounds of the formula (I)-AAA wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R¹ is imidazolyl substituted with R¹¹ or R¹²; and Y, R², R³ and R⁴ are as defined herein.

A compound of the formula AAA1 may be prepared by known methods such as those described in the scientific literature (WO2007/124369). A compound of the formula AAA1 may be treated with an alkylmagnesium halide such as ethylmagnesium chloride and a sulfonating agent such as sulfur dioxide, followed by treatment with a chlorinating agent such as N-chlorosuccinimide, in a solvent such as THF, to afford a compound of the formula AAA2. A compound of the formula II1 may be sulfonylated with a sulfonyl chloride of the formula AAA2 to afford a compound of the formula AAA3. The R² group of the present invention may be installed as previously described herein to afford a compound of the formula AAA4 Amino deprotection of a compound of the formula AAA4 using conventional chemistry known to one skilled in the art provides a compound of the formula AAA5, wherein R_(AAA) is hydrogen. A compound of the formula AAA5 may be converted to a compound of the formula (I)-AAA using chemistry previously described herein. Alternatively, a compound of AAA5 wherein R_(AAA) is hydrogen may be alkylated to form a compound of the formula AAA5 wherein R_(AAA) is C₁₋₃ alkyl, via treatment with a base such as DBU or potassium carbonate; and an electrophile such as iodo(C₁₋₃)alkane or dimethyl sulfate; in a solvent such as DMF. A compound of the formula AAA5 wherein R_(AAA) is C₁₋₃ alkyl may be converted to a compound of the formula (I)-AAA using chemistry previously described herein.

Scheme BBB illustrates a route for the synthesis of compounds of the formula (I)-BBB wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R¹ is cyclohexyl substituted at the 4-position with one substitutent selected from C₁₋₄ alkoxycarbonyl or carboxy; and Y, R², R³ and R⁴ are as defined herein.

A compound of the formula BBB6 may be prepared by known methods such as those described in the scientific literature (Can. J. Chem., 64(16), 1986, 2184). A compound of the formula BBB1, may be treated with thiophosgene in an aprotic non-polar solvent, such as carbon tetrachloride (J. Org. Chem. 43 (2), 1978, 337-339), to afford a compound of the formula BBB2. A compound of the formula BBB2 may be treated with cyclohexa-1,3-diene in a solvent, such as benzene (J. Org. Chem. 45, 1980, 3713-3716), to afford a compound of the formula BBB3. Reduction of the alkenyl group of formula BBB3 may be achieved using a catalyst, such as palladium, and a hydrogen source in a solvent such as ethyl acetate, to afford a compound of the formula BBB4. A compound of the formula BBB4 may be treated with an acid catalyst, such as sulfuric acid, in methanol to afford a compound of the formula BBB5. A compound of the formula BBB5 may be treated with chorine gas in appropriate solvents such as acetic acid-water or dichloromethane-water to afford a compound of the formula BBB6. A compound of the formula BBB7 may be sulfonylated with a sulfonyl chloride of the formula BBB6 to afford a compound of the formula BBB8. A compound of formula BBB8 can be converted to a compound of formula (I)-BBB using chemistry previously described herein. A compound of the formula BBB9 may be treated with hydroxide to effectively epimerize a stereocenter of the cyclohexyl ring, affording a mixture of stereoisomers of the formula BBB10. Saponification of the esters using chemistry described herein affords the compounds of the formula (I)-BBB1. Pure stereoisomers of the formula BBB10 or (I)-BBB1 may be isolated using convention chromatographic techniques.

Scheme CCC illustrates a route for the synthesis of compounds of the formula (I)-CCC wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; R¹ is cyclohexyl substituted at the 4-position with one substitutent selected from cyano, aminocarbonyl, R¹¹, or R¹²; and Y, R², R³ and R⁴ are as defined herein.

A compound of the formula (I)-BBB1 may be converted to a compound of the formula (I)-CCC by the action of a reagent such as HBTU, CDI or HATU, followed by the addition of gaseous ammonia. A compound of the formula (I)-CCC may be converted to a compound of the formula (I)-CCC1 by the action of reagents such as trifluoroacetic anhydride in pyridine; in a solvent such as dichloromethane. The cyano group of a compound of the formula (I)-CCC1 may be converted to R¹¹ and R¹² groups of the present invention using synthetic methods described in the previous schemes to afford a compound of the formula (I)-CCC2.

Scheme DDD illustrates a route for the synthesis of compounds of the formula (I)-DDD wherein A and B are C(R⁵) and C(R⁶) respectively; G is S; R¹ is R¹¹ or R¹²; and Y, R², R³ and R⁴ are as defined herein.

A compound of the formula DDD1 may be prepared using chemistry previously described herein. A compound of the formula DDD1 may be converted to a compound of the formula DDD2 using sodium cyanide and a polar aprotic solvent such as DMF or DMSO. The cyano group of a compound of the formula DDD2 may be converted to R¹¹ and R¹² groups of the present invention using synthetic methods described in the previous schemes to afford a compound of the formula (I)-DDD.

Scheme EEE illustrates a route for the synthesis of compounds of formula (I)-EEE wherein A and B are C(R⁵) and C(R⁶), respectively; G is S; Y_(EEE) is hydrogen, alkyl, C₃₋₈ cycloalkyl, or trifluoromethyl; and R¹, R², R³ and R⁴ are as defined herein.

A compound of the formula EEE1 is either commercially available or may be prepared by known methods such as those described in the scientific literature. A compound of the formula EEE1 wherein X_(EEE) is chloro or fluoro may be reacted with an R-substituted thioglycolate (wherein R is C₁₋₆alkyl) in the presence of base to afford a compound of the formula EEE2, which may be saponified to afford a compound of the formula EEE3 using conventional chemistry known to one skilled in the art. Using synthetic methods outlined in scheme A, a compound of the formula EEE3 may be converted to compounds of the formula (I)-EEE.

Scheme FFF illustrates a route for the synthesis of compounds of the formula (I)-FFF wherein Y_(FFF) is other than bromo or iodo; G is S; and R¹ is C₆₋₁₀aryl substituted with an optionally substituted phenyl; or R¹ is phenyl substituted with a heteroaryl; R² is a substituent that does not include bromo or iodo; R³ is other than bromo; and R⁴ and R⁶ are as defined herein.

A compound of the formula FFF1 wherein X_(FFF) is bromo or iodo can then prepared according to the chemistry described herein. A compound of the formula FFF1 may be coupled with a suitably substituted aryl boronic acid, aryl trialkylsilane, aryl tin reagent, and the like of the formula FFF2 (wherein M is the reactive coupling functionality) by a variety of coupling reactions that are well known to those versed in the art, such as a palladium-catalyzed Suzuki cross-coupling reaction. The reaction may be carried out in the presence or absence of added ligands for palladium; in the presence of a suitable base such as cesium carbonate, potassium carbonate, or sodium carbonate; in an organic solvent such as ethanol, THF, DMF, toluene, and the like. One skilled in the art will recognize that in some instances it may be favorable to reverse the coupling partners such that ring F bears the reactive coupling functionality M, and the Ar ring of the formula FFF2 bears halide X_(FFF).

Scheme GGG illustrates a route for the synthesis of compounds of the formula (I)-GGG wherein Y_(GGG) is other than bromo or iodo; G is S; and R¹ is heteroaryl substituted with an optionally substituted phenyl or heteroaryl; R² is a substituent that does not include bromo or iodo; R³ is other than bromo; and R⁴ and R⁶ are as defined herein.

A compound of the formula GGG1 wherein X_(GGG) is bromo or iodo can then prepared according to the chemistry described herein. A compound of the formula GGG1 may be coupled with a suitably substituted heteroaryl boronic acid, heteroaryl trialkylsilane, heteroaryl tin reagent, and the like of the formula GGG2 (wherein M is the reactive coupling functionality) by a variety of coupling reactions that are well known to those versed in the art, such as a palladium-catalyzed Suzuki cross-coupling reaction. The reaction may be carried out in the presence or absence of added ligands for palladium; in the presence of a suitable base such as cesium carbonate, potassium carbonate, or sodium carbonate; in an organic solvent such as ethanol, THF, DMF, toluene, and the like. One skilled in the art will recognize that in some instances it may be favorable to reverse the coupling partners such that ring G bears the reactive coupling functionality M, and the HET ring of the formula GGG2 bears halide X_(GGG).

Scheme HHH illustrates a route for the synthesis of compounds of the formula (I)-HHH wherein R¹ is phenyl substituted at the 3- or 4-position with imidazolyl substituted with an 2-aminoethyl, 2-(C₁₋₂ alkylamino)ethyl, or 2-(di(C₁₋₂ alkyl)amino)ethyl substitutent; R_(H) and R_(H1) are independently hydrogen or C₁₋₂ alkyl; or R_(H) and R_(H1) are taken together with the nitrogen atom to which it is attached to form a 5 or 6 membered ring optionally containing one additional heteroatom selected from nitrogen, oxygen, or sulfur; and wherein the ring formed by di(C₁₋₂ alkyl)amino is optionally substituted with C₁₋₃alkyl; and A, B, G, Y, R², R³, and R⁴ are as defined herein.

A compound of the formula HHH1 is either commercially available or may be prepared by known methods such as those described in the scientific literature. The nitrogen heteroatom of a compound of the formula HHH1 may be protected with an appropriate protecting group (P) such as a trityl group, to afford a compound of the formula HHH2. A compound of the formula HHH2 may be treated with a strong base such as n-butyllithium followed by the addition of ethylchloroformate in an organic aprotic solvent afford an aldehyde of the formula HHH3 (Synlett 1999, No 12, 1875-1878). A compound of the formula HHH3 may undergo a reductive alkylation with an amine of the formula NHR_(H)R_(H1) in the presence of a hydride source such as sodium borohydride, sodiumtriacetoxyborohydride, and the like, in an alcoholic solvent such as methanol to afford a compound of the formula HHH4 Conventional removal of the nitrogen protecting group affords a compound of the formula HHH5. A compound of the formula UU3 may be coupled with a compound of the formula HHH5 in an organic solvent such as DMSO and a base such as K₂CO₃ to afford a compound of the formula (I)-HHH.

Compounds of Formula (I) that are chiral may be separated into their enantiomers by chromatography on a chiral stationary phase. Alternatively, basic or acidic compounds and intermediates to compounds of the present invention may be converted to diastereomeric salts by mixture with a chiral acid or base, respectively, and resolved into their enantiomers by fractional crystallization.

It is generally preferred that the respective product of each process step be separated from other components of the reaction mixture and subjected to purification before its use as a starting material in a subsequent step. Separation techniques typically include evaporation, extraction, precipitation and filtration. Purification techniques typically include column chromatography (Still, W. C. et. al., J. Org. Chem. 1978, 43, 2921), thin-layer chromatography, crystallization and distillation. The structures of the final products, intermediates and starting materials are confirmed by spectroscopic, spectrometric and analytical methods including nuclear magnetic resonance (NMR), mass spectrometry (MS) and liquid chromatography (HPLC). In the descriptions for the preparation of compounds of this invention, ethyl ether, tetrahydrofuran and dioxane are common examples of an ethereal solvent; benzene, toluene, hexanes and heptanes are typical hydrocarbon solvents and dichloromethane and dichloroethane are representative halogenated hydrocarbon solvents. In those cases where the product is isolated as the acid addition salt the free base may be obtained by techniques known to those skilled in the art. In those cases in which the product is isolated as an acid addition salt, the salt may contain one or more equivalents of the acid. Enantiomers of the compounds of the present invention may be separated using chiral HPLC.

SPECIFIC EXAMPLES

Reagents were purchased from commercial sources. Microanalyses were performed at Quantitative Technologies, Inc., Whitehouse, N.J. and are expressed in percentage by weight of each element per total molecular weight. Nuclear magnetic resonance (NMR) spectra for hydrogen atoms were measured in the indicated solvent with (TMS) as the internal standard on a Bruker Avance (300, 400, or 500 MHz) spectrometer. The values are expressed in parts per million downfield from TMS. The mass spectra (MS) were determined on a Micromass Platform LC spectrometer or an Agilent 1100 series LC/MSD spectrometer using an electrospray technique. Unless otherwise noted, the materials used in the examples were obtained from readily available commercial suppliers or synthesized by standard methods known to one skilled in the art of chemical synthesis. The substituent groups, which vary between examples, are hydrogen unless otherwise noted. Where reactions were carried out in a microwave reactor, a Personal Chemistry Smith Synthesizer™ was used.

Example 1

Benzo[b]thiophen-2-yl-carbamic acid tert-butyl ester (1-B)

A solution of compound 1-A (14.4 g, 80.6 mmol), N,N-diisopropylethylamine (15.5 mL, 88.6 mmol) and diphenylphosphoryl azide (20.8 mL, 96.7 mmol) in t-butanol (150 mL) was heated at reflux for 8 h. The solvent was evaporated in vacuo, and the residue purified by flash column chromatography on silica gel, eluting with dichloromethane, to afford compound 1-B as a colorless solid (18.9 g, 94%). ¹H-NMR (DMSO-d₆): δ 1.50 (s, 9H), 6.78 (s, 1H), 7.16 (d of d, 1H), 7.27 (d of d, 1H), 7.58 (d, 1H), 7.77 (d, 1H), 10.70 (br s, 1H); MS: m/z 250.2 (MH⁺).

Benzo[b]thiophen-2-ylamine hydrochloride (1-C)

Compound 1-B (1.45 g, 5.81 mmol) was added to a solution of HCl in dioxane (4 N, 20 mL), and the mixture was stirred at rt until all the starting material was consumed. The mixture was diluted with diethyl ether, the product collected by filtration, and washed with diethyl ether, to afford compound 1-C as an off-white solid (0.89 g, 83%). ¹H-NMR (DMSO-d₆): δ 6.43 (s, 1H), 6.8-7.2 (br s, 3H) superimposed on 7.05 (m, 1H) and 7.20 (m, 1H), 7.45 (d, 1H), 7.66 (d, 1H); MS: m/z 150.1 (MH⁺).

N-Benzo[b]thiophen-2-yl-benzenesulfonamide (1-D)

Benzenesulfonyl chloride (0.661 mL, 5.15 mmol) was added to a solution of compound 1-C (0.87 g, 4.69 mmol) in pyridine (10 mL) at 0° C. The ice bath was removed and the solution was stirred at ambient temperature for 2 h. The solvent was evaporated in vacuo, and the residue was partitioned between 2 N HCl and dichloromethane. The organic layer was dried over magnesium sulfate and the solvent evaporated in vacuo. The residue was pre-absorbed on silica gel and purified by flash column chromatography, eluting with a gradient of ethyl acetate (10-50%) in heptane, to afford compound 1-D as a colorless solid (1.19 g, 88%). ¹H-NMR (CDCl₃): δ 6.96 (s, 1H), 7.25-7.34 (m, 2H), 7.44-7.49 (m, 2H), 7.55-7.66 (m, 3H), 7.84-7.88 (m, 2H); MS: m/z 290.1 (MH⁺).

Compound 1 N-Benzo[b]thiophen-2-yl-N-(3,4-difluoro-benzyl)-benzenesulfonamide

Sodium hydride (60% in oil, 100 mg, 2.48 mmol) was added to a solution of compound 1-D (655 mg, 2.26 mmol) in DMF (8 mL) at 0° C. and the resultant mixture was stirred at 0° C. for 15 min. 3,4-Difluorobenzylbromide (0.318 mL, 2.48 mmol) was added to the reaction mixture, and the resultant solution was stirred at ambient temperature overnight. Water was added to the solution, and the product was extracted into ethyl acetate. The organic layer was washed with water (3×), brine, dried over sodium sulfate, filtered, and the solvent evaporated in vacuo. The residue was purified on silica gel by flash column chromatography eluting with a gradient of ethyl acetate (0-40%) in heptane, to afford compound 1 as a colorless solid (570 mg, 61%). ¹H-NMR (DMSO-d₆): δ 4.74 (s, 2H), 7.00-7.10 (s superimposed on m, 3H), 7.15-7.21 (m, 1H), 7.26-7.36 (m, 2H), 7.49-7.54 (m, 2H), 7.62-7.67 (m, 3H), 7.73-7.78 (m, 2H); MS: m/z 416.1 (MH⁺).

Following the procedure described above for Example 1 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 2 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-1-methyl-1H-imidazole-4-sulfonamide

¹H-NMR (DMSO-d₆): δ 2.02 (s, 3H), 3.72 (s, 3H), 4.82 (s, 2H), 7.10-7.17 (m, 1H), 7.32-7.41 (m, 4H), 7.63-7.68 (m, 1H), 7.79-7.84 (m, 1H), 7.88 (s, 1H), 8.00 (s, 1H); MS: m/z 434.26 (MH⁺).

Compound 3 N-Benzo[b]thiophen-2-yl-N-(3-fluoro-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.76 (s, 2H), 6.94-6.98 (m, 3H), 7.27-7.32 (m, 4H), 7.48-7.53 (d of d, 2H), 7.60-7.64 (m, 3H), 7.66-7.78 (m, 2H); MS: m/z 398.1 (MH⁺).

Compound 4 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-benzyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.81 (s, 2H), 7.10 (t, 2H), 7.28-7.32 (m, 2H), 7.46-7.52 (m, 2H), 7.67-7.72 (m, 3H), 7.82 (t, 1H), 7.90-7.97 (m, 3H); MS: m/z 432.1 (MH⁺).

Compound 5 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-quinolin-8-ylmethyl-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 5.56 (s, 2H), 7.43 (m, 3H), 7.57 (t, 1H), 7.63-7.74 (m, 3H), 7.78-7.96 (m, 6H), 8.31 (d of d, 1H), 8.75 (d of d, 1H); MS: m/z 465.1 (MH⁺).

Compound 6 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.86 (s, 2H), 7.29 (d, 2H), 7.40-7.51 (m, 4H), 7.67-7.72 (m, 3H), 7.80 (t, 1H), 7.90-7.97 (m, 3H); MS: m/z 498.1 (MH⁺).

Compound 7 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.93 (s, 2H), 7.41-7.54 (m, 3H), 7.65-7.73 (m, 5H), 7.83 (t, 1H), 7.92-8.00 (m, 3H); MS: m/z 500.1 (MH⁺).

Compound 8 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-trifluoromethyl-benzyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.94 (s, 2H), 7.46-7.60 (m, 4H), 7.66-7.72 (m, 5H), 7.83 (t, 1H), 7.91-7.99 (m, 3H); MS: m/z 482.1 (MH⁺).

Compound 9 N-(Benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-pyridine-2-sulfonamide

¹H-NMR (DMSO-d₆): δ 5.10 (s, 2H), 7.17 (s, 1H), 7.25-7.32 (m, 3H), 7.37-7.46 (m, 2H), 7.69-7.73 (m, 1H), 7.76-7.82 (m, 2H), 7.95 (d, 1H), 8.09-8.14 (m, 1H), 8.89 (d, 1H); MS: m/z 417.1 (MH⁺).

Compound 10 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(quinolin-8-ylmethyl)-1-methyl-1H-imidazole-4-sulfonamide

¹H-NMR (DMSO-d₆): δ 2.10 (s, 3H), 3.78 (s, 3H), 5.63 (s, 2H), 7.27-7.35 (m, 2H), 7.48-7.62 (m, 3H), 7.70-7.78 (m, 1H), 7.83-7.97 (m, 3H), 8.04 (s, 1H), 8.35 (d, 1H), 8.87 (d, 1H); MS: m/z 449.1 (MH⁺).

Compound 11 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-1-methyl-1H-imidazole-4-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.96 (s, 3H), 3.73 (s, 3H), 4.85 (s, 2H), 7.28 (d, 2H), 7.32-7.48 (m, 4H), 7.61-7.65 (m, 1H), 7.79-7.83 (m, 1H) 7.86 (s, 1H), 7.99 (s, 1H); MS: m/z 482.1 (MH⁺).

Compound 12 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-pyridine-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.98 (s, 3H), 4.81 (br s, 2H), 7.13-7.17 (m, 1H), 7.33-7.42 (m, 4H), 7.68-7.76 (m, 2H), 7.82-7.88 (m, 1H), 8.27-8.31 (m, 1H), 8.97 (d of d, 1H), 9.02 (d, 1H); MS: m/z 431.1 (MH⁺).

Compound 13 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-pyridine-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.92 (s, 3H), 4.83 (br s, 2H), 7.30 (d, 2H), 7.36-7.46 (m, 4H), 7.67-7.76 (m, 2H), 7.83-7.87 (m, 1H), 8.28 (d, 1H), 8.97 (d, 1H), 9.01 (d, 1H); MS: m/z 479.1 (MH⁺).

Compound 14 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(quinolin-8-ylmethyl)-pyridine-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.83 (s, 3H), 5.51 (s, 2H), 7.29-7.38 (m, 2H), 7.47-7.53 (m, 2H), 7.55-7.60 (m, 1H), 7.70-7.80 (m, 3H), 7.90 (d, 1H), 8.34 (d, 2H), 8.80 (d, 1H), 8.97 (d, 1H), 9.02 (d, 1H); MS: m/z 446.1 (MH⁺).

Compound 15 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-thiophene-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.99 (s, 3H), 4.76 (br s, 2H), 7.10-7.16 (m, 1H), 7.28-7.45 (m, 4H), 7.49-7.51 (m, 1H), 7.63-7.70 (m, 1H), 7.81-7.85 (m, 1H), 7.89-7.92 (m, 1H), 8.37-8.38 (m, 1H); MS: m/z 451.0 (MH⁺).

Compound 16 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-thiophene-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.94 (s, 3H), 4.78 (br s, 2H), 7.12 (d, 1H), 7.21-7.41 (m, 4H), 7.49-7.51 (m, 1H), 7.64-7.68 (m, 1H), 7.82-7.85 (m, 1H), 7.89-7.92 (m, 1H), 8.37-8.38 (m, 1H); MS: m/z 484.0 (MH⁺).

Compound 17 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(quinolin-8-ylmethyl)-thiophene-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.94 (s, 3H), 5.50 (s, 2H), 7.30-7.33 (m, 2H), 7.49-7.60 (m, 3H), 7.69-7.77 (m, 1H), 7.82-7.91 (m, 4H), 8.32-8.39 (m, 2H), 8.83-8.85 (m, 1H); MS: m/z 451.0 (MH⁺).

Compound 18 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzo[b]thiophene-2-sulfonamide

¹H-NMR (DMSO-d₆): δ 2.03 (s, 3H), 4.86 (br s, 2H), 7.14-7.20 (m, 1H), 7.30-7.47 (m, 3H), 7.54-7.75 (m, 3H), 7.82-7.87 (m, 1H), 8.10 (d, 1H), 8.20 (d, 1H), 8.26 (s, 1H); MS: m/z 486.1 (MH⁺).

Compound 19 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(quinolin-8-ylmethyl)-benzo[b]thiophene-2-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.97 (s, 3H), 5.60 (s, 2H), 7.30-7.35 (m, 2H), 7.47-7.65 (m, 6H), 7.73-7.78 (m, 1H), 7.83 (d, 1H), 7.89 (d, 1H), 8.12 (d, 1H), 8.21 (d, 1H), 8.27 (s, 1H), 8.32 (d of d, 1H), 8.76-8.79 (m, 1H); MS: m/z 501.1 (MH⁺).

Compound 20 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-quinoline-8-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.74 (s, 3H), 5.29 (br s, 2H), 5.55 (br s, 1H), 7.16-7.22 (m, 1H), 7.27-7.44 (m, 4H), 7.56-7.61 (m, 1H), 7.64-7.70 (m, 2H), 7.82-7.87 (m, 1H), 8.23 (d of d, 1H), 8.36-8.40 (m, 1H), 8.65-8.67 (m, 1H), 9.28-9.30 (m, 1H); MS: m/z 481.2 (MH⁺).

Compound 21 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-quinoline-8-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.70 (s, 3H), 5.32 (br s, 2H), 5.77 (br s, 1H), 7.26-7.35 (m, 4H), 7.44 (d, 2H), 7.54-7.59 (m, 1H), 7.62-7.69 (m, 2H), 7.83-7.87 (m, 1H), 8.22 (d of d, 1H), 8.38 (d of d, 1H), 8.66 (d of d, 1H), 9.28-9.33 (m, 1H); MS: m/z 529.2 (MH⁺).

Compound 22 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(quinolin-8-ylmethyl)-quinoline-8-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.64 (s, 3H), 6.06 (s, 2H), 7.21-7.25 (m, 2H), 7.43-7.48 (m, 2H), 7.58-7.69 (m, 3H), 7.83-7.87 (m, 1H), 7.91-7.98 (m, 2H), 8.24-8.39 (m, 3H), 8.65-8.72 (m, 2H), 9.29-9.30 (m, 1H); MS: m/z 496.2 (MH⁺).

Compound 23 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(3-fluoro-benzyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.85 (s, 2H), 7.04-7.15 (m, 2H), 7.27-7.37 (m, 1H), 7.46-7.52 (m, 2H), 7.66-7.97 (m, 8H); MS: m/z 432.1 (MH⁺).

Compound 24 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.83 (s, 2H), 7.10-7.18 (m, 1H), 7.27-7.38 (m, 2H), 7.47-7.54 (m, 2H), 7.66-7.75 (m, 3H), 7.80-7.85 (m, 1H), 7.89-7.99 (m, 3H); MS: m/z 450.1 (MH⁺).

Compound 25 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-methoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.97 (s, 3H), 3.82 (s, 3H), 4.75 (br s, 2H), 7.08-7.15 (m, 1H), 7.26-7.45 (m, 7H), 7.60 (t, 1H), 7.66-7.70 (m, 1H), 7.82-7.88 (m, 1H); MS: m/z 460.1 (MH⁺).

Compound 26 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-methoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.98 (s, 3H), 3.88 (s, 3H), 4.70 (br s, 2H), 7.08-7.21 (m, 3H), 7.26-7.41 (m, 4H), 7.65-7.70 (m, 1H), 7.77-7.85 (m, 3H); MS: m/z 460.2 (MH⁺).

Compound 27 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-isoquinoline-5-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.74 (s, 3H), 4.89 (br s, 2H), 7.06-7.13 (m, 1H), 7.24-7.42 (m, 4H), 7.58-7.64 (m, 1H), 7.75-7.80 (m, 1H), 7.88 (t, 1H), 8.33 (d, 1H), 8.45 (d, 1H), 8.56-8.61 (m, 2H), 9.59 (s, 1H); MS: m/z 481.2 (MH⁺).

Compound 28 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-isoquinoline-5-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.76 (s, 3H), 6.03 (s, 2H), 7.25-7.72 (m), 8.25 (t, 1H), 8.76-8.92 (m, 4H), 10.47 (s, 1H); MS: m/z 529.1 (MH⁺).

Compound 29 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(quinolin-8-ylmethyl)-isoquinoline-5-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.47 (s, 3H), 5.54 (s, 2H), 7.27-7.52 (m, 5H), 7.60 (d, 1H), 7.72-7.76 (m, 1H), 7.87 (d, 1H), 8.01 (t, 1H), 8.30-8.35 (m, 1H), 8.61-8.68 (m, 3H), 8.71-8.76 (m, 2H), 9.87 (s, 1H); MS: m/z 496.2 (MH⁺).

Compound 30 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-quinoline-6-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.97 (s, 3H), 4.85 (br s, 2H), 7.12-7.20 (m, 1H), 7.29-7.42 (m, 4H), 7.64-7.71 (m, 1H), 7.76-7.85 (m, 2H), 8.21 (d of d, 1H), 8.35 (d, 1H), 8.74-8.80 (m, 2H), 9.19-9.21 (m, 1H); MS: m/z 481.2 (MH⁺).

Compound 31 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-quinoline-6-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.92 (s, 3H), 4.87 (s, 2H), 7.27-7.46 (m, 6H), 7.64-7.69 (m, 1H), 7.77-7.87 (m, 2H), 8.22 (d of d, 1H), 8.37 (d, 1H), 8.75-8.83 (m, 2H), 9.22 (d of d, 1H); MS: m/z 529.2 (MH⁺).

Compound 32 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(quinolin-8-ylmethyl)-quinoline-6-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.84 (s, 3H), 5.57 (s, 2H), 7.27-7.34 (m, 2H), 7.45-7.59 (m, 3H), 7.70-7.90 (m, 4H), 8.21 (d of d, 1H), 8.29 (d, 2H), 8.68-8.73 (m, 2H), 8.76 (d of d, 1H), 9.15 (d of d, 1H); MS: m/z 496.2 (MH⁺).

Compound 33 N-(Benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-pyridine-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 4.94 (s, 2H), 7.17-7.25 (m, 2H), 7.30-7.44 (m, 4H), 7.68-7.77 (m, 2H), 7.80-7.87 (m, 1H), 8.21-8.26 (m, 1H), 8.94 (d of d, 1H), 8.98 (d, 1H); MS: m/z 417.0 (MH⁺).

Compound 34 N-Benzo[b]thiophen-2-yl-N-(3,4-difluoro-benzyl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 3.28 (s, 3H), 4.19 (s, 2H), 7.18-7.24 (m, 1H), 7.31-7.45 (m, 5H), 7.73-7.78 (m, 1H), 7.82-7.89 (m, 1H); MS: m/z 354.1 (MH⁺).

Compound 35 N-(Benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.32 (t, 3H), 3.44 (q, 2H), 4.97 (s, 2H), 7.17-7.24 (m, 1H), 7.30-7.46 (m, 5H), 7.71-7.78 (m, 1H), 7.82-7.87 (m, 1H); MS: m/z 368.1 (MH⁺).

Compound 36 N-(Benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-propane-1-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.01 (t, 3H), 1.72-1.87 (m, 2H), 3.37-3.44 (m, 2H), 4.95 (s, 2H), 7.16-7.23 (m, 1H), 7.30-7.46 (m, 5H), 7.70-7.76 (m, 1H), 7.81-7.88 (m, 1H); MS: m/z 382.2 (MH⁺).

Compound 37 N-(Benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-butane-1-sulfonamide

¹H-NMR (DMSO-d₆): δ 0.892 (t, 3H), 1.35-1.48 (m, 2H), 1.67-1.79 (m, 2H), 3.40-3.45 (m, 2H), 4.96 (s, 2H), 7.16-7.23 (m, 1H), 7.30-7.45 (m, 5H), 7.71-7.77 (m, 1H), 7.82-7.88 (m, 1H); MS: m/z 396.1 (MH⁺).

Compound 38 N-(3-Fluoro-4-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-thiophene-2-sulfonamide

¹H-NMR (DMSO-d₆): δ 2.01 (s, 3H), 4.87 (br s, 2H), 7.32-7.50 (m, 4H), 7.63-7.73 (m, 3H), 7.83-7.88 (m, 2H), 8.17 (d of d, 1H); MS: m/z 486.1 (MH⁺).

Compound 39 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-pyridine-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.97 (s, 3H), 4.92 (br s, 2H), 7.37-7.53 (m, 3H), 7.63-7.79 (m, 4H), 7.84-7.88 (m, 1H), 8.27-8.32 (m, 1H), 8.97-9.04 (m, 2H); MS: m/z 481.2 (MH⁺).

Compound 40 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.35 (t, 3H), 2.04 (s, 3H), 3.46 (q, 2H), 4.89 (s, 2H), 7.37-7.49 (m, 3H), 7.62-7.71 (m, 3H), 7.85-7.92 (m, 1H); MS: m/z 432.1 (MH⁺).

Compound 41 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.35 (t, 3H), 2.06 (s, 3H), 3.44 (q, 2H), 4.79 (s, 2H), 7.10-7.17 (m, 1H), 7.29-7.44 (m, 4H), 7.67-7.72 (m, 1H), 7.87-7.90 (m, 1H); MS: m/z 382.2 (MH⁺).

Compound 42 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.35 (t, 3H), 1.99 (s, 3H), 3.44 (q, 2H), 4.82 (s, 2H), 7.30 (d, 2H), 7.36-7.43 (m, 4H), 7.65-7.70 (m, 1H), 7.86-7.90 (m, 1H); MS: m/z 430.2 (MH⁺).

Compound 43 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.33 (t, 3H), 3.46 (q, 2H), 5.07 (s, 2H), 7.30-7.40 (m, 3H), 7.50 (t, 1H), 7.70-7.77 (m, 3H) and 7.83-7.88 (m, 1H); MS: m/z 418.0 (MH⁺).

Compound 44 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-N′,N′-dimethylsulfamide

¹H-NMR (DMSO-d₆): δ 2.09 (s, 3H), 2.87 (s, 6H), 4.72 (s, 2H), 7.07-7.14 (m, 1H), 7.27-7.42 (m, 4H), 7.66-7.72 (m, 1H), 7.84-7.91 (m, 1H); MS: m/z 397.0 (MH⁺).

Compound 45 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 3.30 (s, 3H), 5.01 (s, 2H), 7.31-7.38 (m, 2H), 7.40 (s, 1H), 7.49 (t, 1H), 7.70-7.78 (m, 3H), 7.83-7.89 (m, 1H); MS: m/z 404.1 (MH⁺).

Compound 46 N-(Benzo[b]thiophen-2-yl)-N-(4-chloro-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.76 (s, 2H), 7.00 (s, 1H), 7.21-7.32 (m, 6H), 7.48-7.53 (m, 2H), 7.61-7.66 (m, 3H), 7.76-7.80 (m, 2H); MS: m/z 414.0 (MH⁺).

Compound 47 N-(Benzo[b]thiophen-2-yl)-N-(2-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.71 (s, 3H), 4.90 (s, 2H), 6.76-6.78 (d, 1H), 6.86-6.90 (t, 1H), 7.01 (s, 1H), 7.17-7.22 (m, 1H), 7.22-7.32 (m, 3H), 7.42-7.51 (m, 3H), 7.58-7.64 (m, 2H), 7.77-7.82 (d, 2H); MS: m/z 410.1 (MH⁺).

Compound 48 N-(Benzo[b]thiophen-2-yl)-N-(3-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.74 (s, 3H), 4.78 (s, 2H), 6.75-6.78 (m, 1H), 6.88-6.91 (m, 2H), 7.01 (s, 1H), 7.15-7.19 (m, 1H), 7.25-7.31 (m, 2H), 7.48-7.52 (m, 2H), 7.59-7.64 (m, 3H), 7.76-7.78 (d, 2H); MS: m/z 410.1 (MH⁺).

Compound 49 N-(Benzo[b]thiophen-2-yl)-N-(4-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.74 (s, 3H), 4.74 (s, 2H), 6.76-6.81 (d, 2H), 6.97 (s, 1H), 7.21-7.31 (m, 4H), 7.47-7.51 (m, 2H), 7.59-7.65 (m, 3H), 7.76-7.80 (d, 2H); MS: m/z 410.1 (MH⁺), 432.0 (MNa⁺).

Compound 50 N-(Benzo[b]thiophen-2-yl)-N-(2-fluoro-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.92 (s, 2H), 6.92-6.97 (m, 1H), 7.01 (s, 1H), 7.06-7.11 (m, 1H), 7.19-7.31 (m, 3H), 7.48-7.53 (m, 3H), 7.60-7.65 (m, 3H), 7.77-7.81 (d, 2H); MS: m/z 398.1 (MH⁺).

Compound 51 N-(Benzo[b]thiophen-2-yl)-N-(3-nitro-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.89 (s, 2H), 7.05 (s, 1H), 7.26-7.31 (m, 2H), 7.46-7.54 (m, 3H), 7.62-7.68 (m, 3H), 7.74-7.79 (m, 3H), 8.05-8.19 (m, 2H); MS: m/z 425.1 (MH⁺).

Compound 52 N-(Benzo[b]thiophen-2-yl)-N-(pyridin-2-ylmethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 5.17 (s, 2H), 7.07 (s, 1H), 7.26-7.32 (m, 3H), 7.38-7.43 (m, 1H), 7.48-7.55 (m, 2H), 7.60-7.67 (m, 2H), 7.77-7.79 (m, 2H), 7.87-7.89 (m, 1H), 7.94-7.98 (m, 1H), 8.59-8.61 (m, 1H); MS: m/z 381.0 (MH⁺).

Compound 53 N-(Benzo[b]thiophen-2-yl)-N-(pyridin-3-ylmethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.97 (s, 2H), 7.07 (s, 1H), 7.32-7.34 (m, 2H), 7.52-7.57 (m, 3H), 7.63-7.71 (m, 3H), 7.76-7.83 (m, 3H), 8.48-8.49 (m, 1H), 8.75-8.76 (m, 1H), 8.83 (s, 1H); MS: m/z 381.0 (MH⁺).

Compound 54 N-(Benzo[b]thiophen-2-yl)-N-(pyridin-4-ylmethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 5.02 (s, 2H), 7.13 (s, 1H), 7.33-7.37 (m, 2H), 7.53-7.57 (m, 2H), 7.63-7.71 (m, 3H), 7.76-7.78 (m, 2H), 7.84-7.88 (m, 2H), 8.81-8.84 (m, 2H); MS: m/z 381.0 (MH⁺).

Compound 55 N-(Benzo[b]thiophen-2-yl)-N-(2-nitro-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 5.29 (s, 2H), 7.11 (s, 1H), 7.27-7.31 (m, 2H), 7.40-7.44 (m, 1H), 7.50-7.54 (m, 2H), 7.61-7.69 (m, 4H), 7.78-7.80 (m, 2H), 7.97-8.03 (m, 2H); MS: m/z 425.1 (MH⁺).

Compound 56 N-(Benzo[b]thiophen-2-yl)-N-(2-trifluoromethoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.93 (s, 2H), 7.01 (s, 1H), 7.15-7.18 (m, 1H), 7.23-7.30 (m, 4H), 7.49-7.53 (m, 2H), 7.59-7.66 (m, 4H), 7.78-7.79 (m, 2H); MS: m/z 464.1 (MH⁺).

Compound 57 N-(Benzo[b]thiophen-2-yl)-N-(3-trifluoromethoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.81 (s, 2H), 7.01 (s, 1H), 7.07-7.09 (m, 1H), 7.19 (s, 1H), 7.25-7.31 (m, 4H), 7.48-7.53 (m, 2H), 7.61-7.66 (m, 3H), 7.76-7.78 (m, 2H); MS: m/z 464.1 (MH⁺).

Compound 58 N-(Benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.80 (s, 2H), 7.01 (s, 1H), 7.10-7.12 (d, 2H), 7.28-32 (m, 2H), 7.35-7.37 (m, 2H), 7.48-7.52 (m, 2H), 7.61-7.65 (m, 3H), 7.75-7.77 (m, 2H); MS: m/z 464.0 (MH⁺).

Compound 59 N-(Benzo[b]thiophen-2-yl)-N-(benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.80 (s, 2H), 6.99 (s, 1H), 7.22-7.28 (m, 5H), 7.31-7.33 (m, 2H), 7.48-7.51 (m, 2H), 7.59-7.64 (m, 3H), 7.77-7.79 (m, 2H); MS: m/z 380.1 (MH⁺).

Compound 60 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.82 (s, 3H), 4.75 (s, 2H), 6.72-6.78 (m, 1H), 6.89-6.94 (m, 1H), 6.98-6.99 (m, 2H), 7.28-7.31 (m, 2H), 7.48-7.53 (m, 2H), 7.61-7.64 (m, 3H), 7.76-7.78 (m, 2H); MS: m/z 428.1 (MH⁺).

Compound 61 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.80 (s, 2H), 7.03 (s, 1H), 7.08-7.14 (m, 1H), 7.28-7.34 (m, 2H), 7.49-7.55 (m, 5H), 7.63-7.68 (m, 3H), 7.75-7.77 (m, 2H); MS: m/z 466.0 (MH⁺).

Compound 62 N-(Benzo[b]thiophen-2-yl)-N-(2-methyl-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.39 (s, 3H), 4.81 (s, 2H), 6.97 (s, 1H), 7.01-7.05 (m, 1H), 7.09-7.12 (m, 2H), 7.20-7.29 (m, 3H), 7.49-7.53 (m, 2H), 7.58-7.66 (m, 3H), 7.77-7.81 (d, 2H); MS: m/z 394.0 (MH⁺).

Compound 63 N-(Benzo[b]thiophen-2-yl)-N-(3-methyl-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.25 (s, 3H), 4.76 (s, 2H), 7.00 (s, 1H), 7.02-7.04 (m, 1H), 7.09-7.16 (m, 3H), 7.47-7.53 (m, 2H), 7.59-7.64 (m, 3H), 7.76-7.78 (m, 2H); MS: m/z 394.0 (MH⁺).

Compound 64 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-fluoro-4-methoxybenzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.98 (s, 3H), 3.97 (s, 3H), 4.87 (s, 2H), 7.35-7.48 (m, 4H), 7.62-7.71 (m, 4H), 7.76-7.88 (m, 2H); MS: m/z 528.0 (MH⁺), 550.0 (MNa⁺).

Compound 65 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzothiazole-6-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.96 (s, 3H), 4.90 (s, 2H), 7.33-7.52 (m, 3H), 7.63-7.70 (m, 3H), 7.78-7.83 (m, 1H), 7.97-8.01 (m, 1H), 8.31-8.42 (d, 1H), 8.91 (s, 1H), 9.77 (s, 1H); MS: m/z 537.0 (MH⁺).

Compound 66 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2-oxo-2,3-dihydro-benzooxazole-6-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.98 (s, 3H), 4.84 (s, 2H), 7.28-7.48 (m, 4H), 7.60-7.70 (m, 4H), 7.81-7.86 (m, 2H), 12.35 (s, 1H); MS: m/z 537.0 (MH⁺).

Compound 67 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl))-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-6-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.97 (s, 3H), 4.79 (m, 4H), 7.20-7.23 (d, 1H), 7.29-7.51 (m, 4H), 7.61-7.72 (m, 3H), 7.81-7.90 (m, 1H), 10.91 (s, 1H); MS: m/z 551.1 (MH⁺).

Compound 68 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-methyl-3,4-dihydro-2H-benzo[1,4]oxazine-7-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.99 (s, 3H), 2.82 (s, 3H), 4.33-4.36 (m, 2H), 4.78 (s, 2H), 6.97-6.91 (d, 1H), 6.98-7.00 (m, 1H), 7.04-7.09 (m, 2H), 7.32-7.46 (m, 3H), 7.59-7.69 (m, 3H), 7.83-7.87 (m, 1H); MS: m/z 551.1 (MH⁺).

Compound 69 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-[1,2,3]thiadiazol-4-yl-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.98 (s, 3H), 4.92 (s, 2H), 7.34-7.51 (m, 3H), 7.65-7.71 (m, 3H), 7.82-7.85 (m, 1H), 8.04-8.06 (d, 2H), 8.44-8.47 (d, 2H), 9.92 (s, 1H); MS: m/z 564.0 (MH⁺), 586.0 (MNa⁺).

Compound 70 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-phenoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.87 (s, 3H), 5.06 (s, 2H), 7.05-7.08 (d, 1H), 7.21-7.39 (m, 6H), 7.43-7.54 (m, 3H), 7.62-7.86 (m, 6H); MS: m/z 572.1 (MH⁺).

Compound 71 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethylbenzyl)-2-carbomethoxypropanesulfonamide

¹H-NMR (DMSO-d₆): δ 2.01 (s, 3H), 2.82-2.89 (t, 2H), 3.65 (s, 3H), 3.71-3.75 (t, 2H), 4.89 (s, 2H), 7.39-7.48 (m, 3H), 7.59-7.71 (m, 3H), 7.84-7.92 (m, 1H); MS: m/z 490.0 (MH⁺), 512.0 (MNa⁺).

Compound 72 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethylbenzyl)-(2,4-dihydroxy-6-methyl-pyrimidine-5-yl)sulfonamide

¹H-NMR (DMSO-d₆): δ 1.94 (s, 3H), 2.08 (s, 3H), 4.98 (s, 3H), 7.34-7.50 (m, 3H), 7.60-7.69 (m, 3H), 7.84-7.92 (m, 1H), 11.66 (s, 1H), 11.85 (s, 1H); MS: m/z 528.0 (MH⁺).

Compound 73 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2-(2,2,2-trifluoro-acetyl)-1,2,3,4-tetrahydro-isoquinoline-8-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.94-1.98 (m, 3H), 3.02-3.09 (m, 2H), 3.80-3.90 (m, 2H), 4.76-4.90 (m, 4H), 7.34-7.53 (m, 4H), 7.60-7.69 (m, 5H), 7.82-7.85 (m, 1H), 7.96 (s, 1H); MS: m/z 631.0 (MH⁺).

Compound 74 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-1,3,5-trimethyl-1H-pyrazole-4-sulfonamide

¹H-NMR (DMSO-d₆): δ 2.04 (s, 6H), 2.18 (s, 3H), 3.72 (s, 3H), 4.76 (s, 2H), 7.34-7.46 (m, 3H), 7.60-7.69 (m, 3H), 7.82-7.89 (m, 1H); MS: m/z 512.0 (MH⁺).

Compound 75 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2,4-dimethyl-thiazole-5-sulfonamide

¹H-NMR (DMSO-d₆): δ 2.04 (s, 3H), 2.29 (s, 3H), 2.71 (s, 3H), 4.83 (s, 2H), 7.35-7.51 (m, 3H), 7.63-7.75 (m, 3H), 7.88-7.92 (m, 1H); MS: m/z 515.0 (MH⁺).

Compound 76 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-6-chloro-pyridine-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 2.01 (s, 3H), 4.83 (s, 2H), 7.35-7.51 (m, 3H), 7.63-7.75 (m, 3H), 7.88-7.92 (m, 2H), 8.31-8.34 (m, 1H), 8.90 (d, 1H); MS: m/z 515.0 (MH⁺).

Compound 77 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2-chloro-pyridine-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.02 (s, 3H), 5.15 (s, 2H), 7.35-7.40 (m, 2H), 7.45-7.75 (m, 5H), 7.82-7.85 (m, 1H), 8.26-8.32 (m, 1H), 8.72-8.77 (m, 1H); MS: m/z 515.0 (MH⁺).

Compound 78 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-thiophene-3-sulfonamide

¹H-NMR (DMSO-d₆): δ 4.98 (s, 2H), 7.19 (s, 1H), 7.31-7.34 (m, 2H), 7.42-7.43 (m, 1H), 7.46-7.51 (m, 1H), 7.68-7.75 (m, 3H), 7.82-7.90 (m, 2H), 8.38-8.39 (m, 1H); MS: m/z 472.0 (MH⁺).

Compound 462 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-N′,N′-dimethylsulfamoyl-benzenesulfonamide

MS: m/z 573.2 (MH⁺).

Compound 825 N-(Benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3,4-difluoro-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.02 (s, 3H), 4.78 (br s, 2H), 7.28 (s, 5H), 7.41 (m, 3H), 7.62 (m, 2H), 7.72 (m, 2H); MS: m/z 452.0 (MNa⁺).

Compound 826 N-(4-Fluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3,4-difluoro-benzenesulfonamide

¹H NMR (CDCl₃) δ 2.02 (s, 3H), 4.72 (br s, 2H), 6.95 (m, 2H), 7.22 (m, 2H), 7.42 (m, 3H), 7.61 (m, 2H), 7.72 (m, 2H); MS: m/z 447.9 (MH⁺), 470.0 (MNa⁺).

Compound 828 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-methoxy-benzyl)-ethanesulfonamide

MS: m/z 380.0 (MH⁺), 402 (MNa⁺).

Compound 829 N-(2-Fluoro-pyridin-4-ylmethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.42 (t, 3H), 2.12 (s, 3H), 3.23 (q, 2H), 4.79 (s, 2H), 6.81 (s, 1H), 7.13 (m, 1H), 7.33 (m, 2H), 7.52 (m, 1H), 7.67 (m, 1H), 8.12 (m, 1H); MS: m/z 365.0 (MH⁺).

Compound 845 3-Fluoro-N-(4-fluoro-benzyl)-4-(4-fluoro-benzyloxy)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

MS: m/z 554.0 (MH⁺), 576.0 (MNa⁺).

Compound 846 N-(Benzyl)-4-benzyloxy-3-fluoro-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

MS: m/z 540.0 (MNa⁺).

Example 2

Compound 79 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-1,2,3,4-tetrahydro-isoquinoline-8-sulfonamide

To a solution of potassium carbonate (0.066 g; 0.48 mmol) in methanol and water (2 mL/2 mL) was added compound 73 (0.06 g; 0.095 mmol) and the reaction was stirred for 18 h at room temperature. The reaction was partitioned between ethyl acetate and water, the layers separated, organics washed with brine, dried over sodium sulfate, flute filtered and the solvent evaporated under reduced pressure. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) eluting with a 40% to 60% MeCN—H₂O gradient to afford compound 79 as a yellow oil (0.035 g, 57%). ¹H-NMR (DMSO-d₆): δ 1.95 (s, 3H), 3.15 (m, 2H), 3.46 (m, 2H), 4.38 (m, 2H), 4.83 (m, 2H), 7.37-7.88 (m, 10H), 9.11 (s, 1H); MS: m/z 535.0 (MH⁺).

Example 3

Compound 80 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(cyclohexylmethyl)-benzenesulfonamide

To triphenylphosphine (0.157 g, 0.60 mmol) dissolved in dry tetrahydrofuran (5 mL) was added a solution of DEAD (0.260 g of 40% solution by weight in toluene, 0.60 mmol). The reaction mixture was stirred at room temperature for 2 minutes, to which was added compound 80-A (0.130 g, 0.40 mmol). Cyclohexyl methanol (0.048 mL, 0.48 mmol) was added and the reaction mixture was stirred at room temperature for 16 h. The reaction mixture was evaporated in vacuo, the residue dissolved in 10 mL of dichloromethane, washed with 10 mL of brine, dried over Na₂SO₄, filtered and the solvent was evaporated in vacuo. The product was purified by flash column chromatography on silica gel eluting with an ethyl acetate-heptane (10-20%) gradient afford compound 80 as a light yellow solid, (0.121 g, 72%). ¹H-NMR (CDCl₃): δ 0.88-1.0 (m, 2H), 1.14-1.27 (m, 3H), 1.30-1.37 (m, 1H), 1.38-1.44 (m, 2H), 1.45-1.48 (m, 1H), 1.62-1.87 (m, 2H), 3.47 (d, 2H), 7.41-7.52 (m, 4H), 7.59-7.64 (m, 1H), 7.70-7.73 (m, 1H), 7.74-7.82 (m, 3H); MS: m/z 420.1 (MH⁺).

Following the procedure described above for Example 3 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 81 N-(2-tert-Butoxy-ethyl)-N-(3-chloro-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.10 (s, 9H), 3.56 (t, 2H), 3.83 (t, 2H), 7.42-7.52 (m, 4H), 7.56-7.68 (m, 1H), 7.70-7.78 (m, 2H), 7.85-7.87 (d, 2H); MS: m/z 446.1 (MNa⁺).

Compound 82 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-[2-(2-oxo-pyrrolidin-1-yl)-ethyl]-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.06-2.16 (m, 2H), 2.48-2.53 (m, 2H), 3.49-3.73 (m, 2H), 3.87-3.91 (m, 2H), 7.44-7.81 (m, 9H); MS: m/z 435.1 (MH⁺).

Compound 83 N-(Butyl)-N-(3-chloro-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.85-0.90 (m, 3H), 1.34-1.55 (m, 4H), 3.62-3.67 (t, 2H), 7.43-7.53 (m, 4H), 7.60-7.68 (m, 1H), 7.69-7.73 (m, 1H), 7.74-7.85 (m, 3H); MS: m/z 380.1 (MH⁺).

Compound 84 N-(Allyl)-N-(3-chloro-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.28-4.31 (m, 2H), 5.08-5.18 (m, 2H), 5.80-5.91 (m, 1H), 7.40-7.50 (m, 2H), 7.52-7.63 (m, 2H), 7.64-7.87 (m, 5H); MS: m/z 364.0 (MH⁺).

Compound 85 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(phenethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.89-2.94 (m, 2H), 3.85-3.90 (m, 2H), 7.13-7.28 (m, 6H), 7.43-7.51 (m, 4H), 7.58-7.82 (m, 4H); MS: m/z 364.0 (MH⁺).

Compound 86 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-[2-(carbo-tert-butoxyamino)ethyl]-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.38 (s, 9H), 3.28-3.32 (t, 2H), 3.75-3.79 (t, 2H), 5.03 (s, 1H, NH), 7.43-7.55 (m, 4H), 7.62-7.85 (m, 5H); MS: m/z 489.1 (MNa⁺).

Compound 87 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(2-dimethylamino-ethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.98 (s, 6H), 3.38-3.42 (t, 2H), 4.06-4.11 (t, 2H), 7.48-7.57 (m, 4H), 7.67-7.82 (m, 5H); MS: m/z 395.1 (MH⁺).

Compound 88 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(2-methanesulfonyl-ethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.03 (s, 3H), 3.40-3.45 (t, 2H), 4.11-4.16 (m, 2H), 7.47-7.57 (m, 4H), 7.66-7.85 (m, 5H); MS: m/z 430.0 (MH⁺).

Compound 89 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-{[1-(carbo-tert-butoxy)pyrrolidin-2-yl]-methyl}-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.29 (s, 9H), 1.94-2.01 (m, 3H), 2.35 (bs, 1H), 3.35-3.36 (m, 2H), 3.61-3.82 (m, 3H), 7.39-7.54 (m, 4H), 7.59-7.71 (m, 2H), 7.75-7.81 (m, 3H); MS: m/z 407.1 (MH⁺-BOC).

Compound 90 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-{[1-(carbo-tert-butoxy)piperidin-4-yl]-methyl}-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.58-1.65 (m, 5H), 1.73 (s, 9H), 3.52-3.54 (bd, 2H), 4.06-4.10 (bd, 2H), 7.44-7.53 (m, 4H), 7.61-7.66 (m, 1H), 7.70-7.77 (m, 1H), 7.78-7.81 (m, 3H); MS: m/z 543.2 (MNa⁺).

Compound 91 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-[2-(2-oxo-imidazolidin-1-yl)-ethyl]-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.37-3.44 (m, 4H), 3.61-3.66 (m, 2H), 3.85-3.89 (m, 2H), 7.43-7.53 (m, 4H), 7.61-7.66 (m, 1H), 7.70-7.83 (m, 4H); MS: m/z 436.4 (MH⁺).

Compound 92 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(2-morpholin-4-yl-ethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.39-2.42 (m, 4H), 2.53-2.57 (m, 2H), 3.57-3.60 (m, 4H), 3.79-3.83 (m, 2H), 7.43-7.53 (m, 3H), 7.71-7.84 (m, 3H), 7.85-7.86 (m, 2H); MS: m/z 437.1 (MH⁺).

Compound 93 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-[2(R)-methyl-2-carbomethoxy-ethyl]-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.27 (s, 3H), 2.34 (s, 3H), 2.61-2.68 (m, 1H), 3.42-4.17 (m, 5H), 7.33-7.40 (m, 2H), 7.42-7.62 (m, 2H), 7.64-7.78 (m, 5H); MS: m/z 404.1 (MH⁺).

Compound 94 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-[2(S)-methyl-2-carbomethoxy-ethyl]-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.26 (s, 3H), 2.33 (s, 3H), 2.61-2.68 (m, 1H), 3.49 (s, 3H), 3.58 (s, 2H), 7.33-7.42 (m, 2H), 7.42-7.61 (m, 2H), 7.62-7.78 (m, 5H); MS: m/z 404.1 (MH⁺).

Compound 95 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2-morpholin-4-yl-ethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.36 (s, 3H), 2.41-2.51 (m, 6H), 3.57-3.74 (m, 6H), 7.33-7.40 (m, 2H), 7.48-7.61 (m, 2H), 7.62-7.66 (m, 3H), 7.69-7.81 (m, 2H); MS: m/z 417.3 (MH⁺).

Compound 96 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2-piperidin-1-yl-ethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.26-1.53 (m, 2H), 2.35 (m, 7H), 2.44-2.49 (t, 2H), 3.52-3.66 (m, 2H), 7.33-7.40 (m, 2H), 7.47-7.52 (m, 2H), 7.59-7.71 (m, 3H), 7.71-7.82 (m, 2H); MS: m/z 415.2 (MH⁺).

Compound 97 N-(Cyclopropylmethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.18-0.20 (m, 2H), 0.43-0.46 (m, 2H), 0.92-1.00 (m, 1H), 2.39 (s, 3H), 7.35-7.39 (m, 2H), 7.48-7.53 (m, 2H), 7.59-7.71 (m, 3H), 7.72-7.81 (m, 2H); MS: m/z 358.2 (MH⁺).

Compound 98 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2-methylsulfanyl-ethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.09 (s, 3H), 2.35 (s, 3H), 2.62-2.67 (m, 2H), 3.74 (bs, 2H), 7.35-7.41 (m, 2H), 7.48-7.55 (m, 2H), 7.60-7.72 (m, 3H), 7.78-7.82 (m, 2H); MS: m/z 378.1 (MH⁺).

Compound 99 N-(2-Methoxy-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.32 (s, 3H), 3.29 (s, 3H), 3.45-3.50 (m, 2H), 3.72 (bs, 2H), 7.35-7.41 (m, 2H), 7.46-7.54 (m, 2H), 7.59-7.73 (m, 3H), 7.79-7.83 (m, 2H); MS: m/z 362.1 (MH⁺).

Compound 100 N-(2-tert-Butoxy-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.10 (s, 9H), 2.30 (s, 3H), 3.46-3.50 (t, 2H), 3.71 (bs, 2H), 7.35-7.39 (m, 2H), 7.47-7.52 (m, 2H), 7.59-7.70 (m, 3H), 7.80-7.83 (m, 2H); MS: m/z 404.2 (MH⁺).

Compound 101 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(carbomethoxy-methyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.10 (s, 9H), 2.33 (s, 3H), 3.70 (s, 3H), 4.42 (s, 2H), 7.35-7.40 (m, 2H), 7.47-7.53 (m, 2H), 7.60-7.70 (m, 3H), 7.79-7.84 (m, 2H); MS: m/z 376.2 (MH⁺).

Compound 102 N-(2,2-Difluoro-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.30 (s, 3H), 3.88 (bs, 2H), 5.83-6.12 (m, 1H), 7.37-7.41 (m, 2H), 7.51-7.56 (m, 2H), 7.65-7.72 (m, 3H), 7.78-7.81 (m, 2H); MS: m/z 368.1 (MH⁺).

Compound 103 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-{[1-(carbo-tert-butoxy)pyrrolidin-2-yl]-methyl}-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.17-1.36 (m, 11H), 1.82-1.97 (m, 2H), 2.32-2.52 (m, 2H), 3.21-3.46 (m, 2H), 3.59-3.74 (m, 1H), 7.31-7.41 (m, 2H), 7.46-7.51 (m, 2H), 7.58-7.79 (m, 5H); MS: m/z 487.2 (MH⁺).

Compound 104

N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(phenethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.31 (s, 3H), 2.82-2.89 (t, 2H), 3.66-3.93 (bs, 2H), 7.10-7.17 (m, 2H), 7.22-7.30 (m, 3H), 7.37-7.42 (m, 2H), 7.46-7.53 (m, 2H), 7.57-7.65 (m, 1H), 7.69-7.78 (m, 4H); MS: m/z 408.1 (MH⁺).

Compound 105 N-(2-Methoxy-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.43-1.47 (t, 3H), 2.42 (s, 3H), 3.23-3.31 (q, 2H), 3.84-3.88 (t, 2H), 7.38-7.41 (m, 2H), 7.69-7.75 (m, 2H); MS: m/z 314.1 (MH⁺).

Compound 106 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.43-1.48 (t, 3H), 2.42 (s, 3H), 2.45-2.52 (m, 2H), 3.18-3.25 (q, 2H), 3.91-3.97 (m, 2H), 7.41-7.44 (m, 2H), 7.70-7.78 (m, 2H); MS: m/z 352.2 (MH⁺).

Compound 107 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(pent-3-ynyl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.43-1.48 (t, 3H), 1.73-1.74 (t, 3H), 2.43 (s, 3H), 3.19-3.27 (q, 2H), 3.78-3.83 (t, 2H), 7.37-7.41 (m, 2H), 7.69-7.75 (m, 2H); MS: m/z 322.2 (MH⁺).

Compound 108 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2-methylsulfanyl-ethyl)-ethane sulfonamide

¹H-NMR (CDCl₃): δ 1.43-1.48 (t, 3H), 2.11 (s, 3H), 2.44 (s, 3H), 2.66-2.71 (t, 2H), 3.20-3.27 (m, 2H), 3.85-3.90 (t, 2H), 7.38-7.42 (m, 2H), 7.70-7.76 (m, 2H); MS: m/z 330.1 (MH⁺).

Compound 109 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5-oxo-(S)-pyrrolidin-2-ylmethyl)-ethane sulfonamide

¹H-NMR (CDCl₃): δ 1.42-1.47 (t, 3H), 2.31-2.37 (m, 4H), 2.44 (s, 3H), 3.17-3.24 (q, 2H), 3.76-3.85 (m, 3H), 5.73 (bs, 1H), 7.41-7.44 (m, 2H), 7.70-7.76 (m, 2H); MS: m/z 353.1 (MH⁺).

Compound 110 N-(2-tert-Butoxy-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.18 (s, 9H), 1.43-1.54 (q, 3H), 2.42 (s, 3H), 3.28-3.35 (q, 2H), 3.48-3.52 (t, 2H), 3.80-3.84 (t, 2H), 5.73 (bs, 1H), 7.37-7.40 (m, 2H), 7.68-7.75 (m, 2H); MS: m/z 356.3 (MH⁺).

Compound 111 N-(2,2-Difluoro-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-ethane sulfon amide

¹H-NMR (CDCl₃): δ 1.44-1.49 (t, 3H), 2.43 (s, 3H), 3.22-3.35 (q, 2H), 3.95-4.06 (t, 2H), 5.78-6.18 (tt, 1H), 7.40-7.43 (m, 2H), 7.71-7.76 (m, 2H); MS: m/z 320.1 (MH⁺).

Compound 112 N-(Cyclopropylmethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 0.00-0.35 (m, 2H), 0.24-0.30 (m, 2H), 0.78-0.88 (m, 1H), 1.19-1.24 (t, 3H), 2.24 (s, 3H), 2.95-3.02 (q, 2H), 3.32-3.34 (td 2H), 7.15-7.19 (m, 2H), 7.48-7.54 (m, 2H); MS: m/z 310.2 (MH⁺).

Compound 113 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2-morpholin-4-yl-ethyl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.43-1.47 (t, 3H), 2.44 (s, 3H), 2.46-2.54 (m, 4H), 3.24-3.33 (q, 2H), 3.65-3.69 (m, 4H), 3.78-3.84 (m, 2H), 7.37-7.43 (m, 2H), 7.69-7.76 (m, 2H); MS: m/z 369.1 (MH⁺).

Compound 114 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-{[1-(carbo-tert-butoxy)pyrrolidin-2-yl]-methyl}-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.20-1.47 (m, 12H), 2.06-2.25 (m, 4H), 2.43 (s, 3H), 3.11-3.41 (m, 4H), 3.60-3.95 (m, 3H), 7.31-7.47 (m, 2H), 7.64-7.78 (m, 2H); MS: m/z 439.2 (MH⁺).

Compound 115 N-(Benzo[b]thiophen-2-yl)-N-(phenethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.83 (t, 2H), 3.89 (t, 2H), 7.19-7.25 (m, 4H), 7.26-7.33 (m, 2H), 7.34-7.41 (m, 2H), 7.58 (t, 2H), 7.66-7.74 (m, 3H), 7.77-7.81 (m, 1H), 7.85-7.90 (m, 1H); MS: m/z 394.2 (MH⁺).

Compound 116 N-(Allyl)-N-(benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H NMR-(DMSO-d₆): δ 4.32 (d, 2H), 5.15 (dd, 1H), 5.26 (dd, 1H), 5.75-5.86 (m, 1H), 7.16 (s, 1H), 7.31-7.38 (m, 2H), 7.62 (t, 2H), 7.71-7.79 (m, 4H), 7.82-7.87 (m, 1H); MS: m/z 330.1 (MH⁺).

Compound 117 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.85 (t, 3H), 1.34 (m, 2H), 1.48 (m, 2H), 3.64 (t, 2H), 7.21 (s, 1H), 7.32-7.39 (m, 2H), 7.61 (t, 2H), 7.70-7.75 (m, 3H), 7.76-7.80 (m, 1H), 7.83-7.88 (m, 1H); MS: m/z 346.1 (MH⁺).

Compound 118 N-(Benzo[b]thiophen-2-yl)-N-(cyclohexylmethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.90-1.02 (m, 2H), 1.03-1.17 (m, 3H), 1.38-1.49 (m, 1H), 1.54-1.60 (m, 1H), 1.61-1.68 (m, 2H), 1.69-1.77 (m, 2H), 3.47 (d, 2H), 7.22 (s, 1H), 7.32-7.39 (m, 2H), 7.60 (t, 2H), 7.68-7.74 (m, 3H), 7.75-7.80 (m, 1H), 7.83-7.87 (m, 1H); MS: m/z 386.2 (MH⁺).

Compound 119 N-(Benzo[b]thiophen-2-yl)-N-(cyclohexyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.79-0.93 (m, 1H), 1.17-1.41 (m, 4H), 1.49 (br d, 1H), 1.64-1.77 (m, 4H), 4.06-4.16 (m, 1H), 7.15 (s, 1H), 7.36-7.43 (m, 2H), 7.64 (t, 2H), 7.69-7.76 (m, 1H), 7.81-7.91 (m, 4H); MS: m/z 372.1 (MH⁺).

Compound 120 N-(Benzo[b]thiophen-2-yl)-N-(2-methylsulfanyl-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.08 (s, 3H), 2.65 (t, 2H), 3.85 (t, 2H), 7.23 (s, 1H), 7.33-7.39 (m, 2H), 7.62 (t, 2H), 7.71-7.81 (m, 4H), 7.84-7.89 (m, 1H); MS: m/z 364.2 (MH⁺).

Compound 121 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(butyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 0.88 (t, 3H), 1.24 (t, 3H), 1.36 (m, 2H), 1.65 (m, 2H), 2.59 (s, 3H), 3.34 (q, 2H), 3.79 (t, 2H), 7.44-7.50 (m, 2H), 7.97-8.02 (m, 1H), 8.06-8.11 (m, 1H); MS: m/z 340.1 (MH⁺).

Compound 122 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(cyclopropylmethyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 0.25-0.31 (m, 2H), 0.50-0.56 (m, 2H), 1.05-1.17 (m, 1H), 1.25 (t, 3H), 2.67 (s, 3H), 3.34 (q, 2H), 3.71 (d, 2H), 7.45-7.51 (m, 2H), 7.97-8.03 (m, 1H), 8.09-8.15 (m, 1H); MS: m/z 338.1 (MH⁺).

Compound 123 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(2-tert-butoxy-ethyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.09 (s, 9H), 1.27 (t, 3H), 2.65 (s, 3H), 3.40 (q, 2H), 3.56 (t, 2H), 3.93 (t, 2H), 7.44-7.50 (m, 2H), 7.97-8.03 (m, 1H), 8.13-8.18 (m, 1H); MS: m/z 384.1 (MH⁺).

Compound 124 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(2-morpholin-4-yl-ethyl)-ethanesulfonamide

MS: m/z 397.2 (MH⁺).

Compound 340 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-pyridin-3-yl-sulfonamide

MS: m/z 347.2 (MH⁺).

Compound 362 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-C-methanesulfonyl-methanesulfonamide

MS: m/z 482.1 (MH⁺).

Compound 363 N-(Butyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-methanesulfonamide

MS: m/z 298.0 (MH⁺).

Compound 364 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-methanesulfonamide

MS: m/z 338.0 (MH⁺).

Compound 365 N-(Cyclopropylmethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-methanesulfonamide

MS: m/z 296.0 (MH⁺).

Compound 366 N-(2-tert-Butoxy-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-methanesulfonamide

MS: m/z 364.0 (MNa⁺).

Compound 382 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-methanesulfonamide

MS: m/z 284.0 (MH⁺).

Compound 422 N-(Butyl)-N-(3-methoxy-benzo[b]thiophen-2-yl)-4-carbomethoxybenzenesulfonamide

Compound 422 was prepared as a solid from Example 1, steps A and B, substituting benzo[b]thiophene-2-carboxylic acid with 3-methoxy-benzo[b]thiophene-2-carboxylic acid and from Example 32, steps E and F. ¹H-NMR (CDCl₃): δ 0.88 (t, 3H), 1.29-1.41 (m, 2H), 1.51-1.61 (m, 2H), 3.54 (t, 2H), 3.98 (s, 3H), 4.09 (s, 3H), 7.33-7.39 (m, 2H), 7.55-7.60 (m, 1H), 7.75-7.78 (m, 1H), 7.92 (d, 2H), 8.17 (d, 2H); MS: m/z 434.1 (MH⁺).

Compound 461 N-(Benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-3-dimethylsulfamoyl-benzenesulfonamide

MS: m/z 493.0 (MH⁺).

Compound 476 N-(Benzo[b]thiophen-2-yl)-4-(bromo)-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

MS: m/z 464, 466 (MH⁺).

Compound 498 N-(Benzo[b]thiophen-2-yl)-4-nitro-N-(3,3,3-tr ifluoro-propyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.43-2.62 (m, 2H), 3.87-3.96 (m, 2H), 7.23 (s, 1H), 7.35-7.46 (m, 2H), 7.67-7.80 (m, 2H), 7.91 (d, 2H), 8.34 (d, 2H).

Compound 564 N-(2-Cyclopropyl-ethyl)-N-(3-isopropyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 458.1 (MH⁺).

Compound 565 N-(3-Isopropyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 514.0 (MH⁺).

Compound 628 N-(2-Cyclopropyl-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ −0.04-0.02 (m, 2H), 0.31-0.51 (m, 2H), 0.55-0.77 (m, 1H), 1.33-1.52 (m, 2H), 2.37 (s, 3H), 3.37-3.82 (m, 2H), 3.94 (s, 3H), 7.30-7.46 (m, 2H), 7.53-7.76 (m, 3H), 7.93 (d, 1H), 8.30 (d, 1H), 8.48 (s, 1H); MS: m/z 430.0 (MH⁺).

Compound 629 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.36 (s, 3H), 2.35-2.55 (m, 2H), 3.67-3.92 (m, 2H), 3.95 (s, 3H), 7.35-7.48 (m, 2H), 7.57-7.76 (m, 3H), 7.90-7.95 (m, 1H), 8.31-8.35 (m, 1H), 8.45-8.47 (m, 1H); MS: m/z 458.0 (MH⁺).

Compound 630 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 472.0 (MH⁺).

Compound 631 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.40-1.57 (m, 2H), 1.58-1.76 (m, 2H), 2.13-2.34 (m, 2H), 2.29 (s, 3H), 2.49-2.52 (m, 2H), 3.42-3.82 (m, 2H), 7.68-7.89 (m, 5H), 8.21-8.34 (m, 2H), 8.44-8.45 (m, 1H); MS: m/z 486.0 (MH⁺).

Compound 817 N-(Benzo[b]thiophen-2-yl)-N-(3-fluoro-propyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.02 (m, 2H), 3.78 (t, 2H), 4.55 (dt, 2H), 7.12 (s, 1H), 7.32 (m, 2H), 7.48 (m, 2H), 7.59 (m, 1H), 7.69 (m, 4H); MS: m/z 350.0 (MH⁺).

Compound 818 N-(2-Fluoro-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.25 (s, 3H), 3.81 (br s, 2H), 4.38 (t, 1H), 4.48 (t, 1H), 7.31 (m, 2H), 7.46 (m, 2H), 7.61 (m, 3H), 7.75 (m, 2H); MS: m/z 350.0 (MH⁺).

Compound 819 N-(3-Fluoro-propyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.88 (m, 2H), 2.29 (s, 3H), 1.81-1.98 (m, 2H), 4.45 (dt, 2H), 7.31 (m, 2H), 7.45 (t, 2H), 7.62 (m, 3H), 7.70 (m, 2H); MS: m/z 364.0 (MH⁺), 386 (MNa⁺).

Compound 823 N-(3-Fluoro-propyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.85 (m, 2H), 2.38 (s, 3H), 3.78 (br s, 2H), 3.98 (s, 3H), 4.52 (dt, 2H), 7.39 (m, 2H), 7.69 (m, 2H), 7.84 (d, 2H), 8.17 (d, 2H); MS: m/z 422.0 (MH⁺), 444 (MNa⁺).

Compound 831 N-(3-Fluoro-propyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3,4-difluoro-benzenesulfonamide

MS: m/z 400.0 (MH⁺), 422 (MNa⁺).

Compound 840 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2,3,5-trifluoro-pyridin-4-ylmethyl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.45 (t, 3H), 2.23 (s, 3H), 3.32 (q, 2H), 5.08 (s, 2H), 7.41 (m, 2H), 7.65 (m, 1H), 7.72 (m, 1H), 7.81 (s, 1H); MS: m/z 401.0 (MH⁺), 423 (MNa⁺).

Compound 841 N-(2-Fluoro-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3,4-difluoro-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.38 (s, 3H), 3.98 (br s, 2H), 4.53 (dt, 2H), 7.34 (m, 1H), 7.53 (m, 2H), 7.62 (m, 1H), 7.72 (m, 3H); MS: m/z 386.0 (MH⁺), 408 (MNa⁺).

Compound 842 N-(Benzo[b]thiophen-2-yl)-N-(3-fluoro-propyl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 408.0 (MH⁺).

Compound 843 N-(Benzo[b]thiophen-2-yl)-N-(2-fluoro-ethyl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 394.0 (MH⁺), 416 (MNa⁺).

Compound 844 N-(Benzo[b]thiophen-2-yl)-N-(2-fluoro-ethyl)-benzenesulfonamide

MS: m/z 336.0 (MH⁺).

Compound 847 N-(Benzo[b]thiophen-2-yl)-N-(2-fluoro-pyridin-4-ylmethyl)-ethane-sulfonamide

MS: m/z 351.0 (MH⁺).

Compound 848 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(2-fluoro-pyridin-4-ylmethyl)-ethansulfonamide

MS: m/z 393.0 (MH⁺), 415 (MNa⁺).

Example 4

(3-Methyl-benzo[b]thiophen-2-yl)-carbamic acid tert-butyl ester (125-B)

A solution of compound 125-A (3.15 g, 16.4 mmol), N,N-diisopropylethylamine (3.15 mL, 18.0 mmol) and diphenyl phosphoryl azide (4.23 mL, 19.7 mmol) in t-butanol (40 mL) was heated at reflux for 8 h. The solvent was evaporated in vacuo, and the residue partitioned between dichloromethane and 1N aqueous sodium hydroxide. The organic layer was applied to a silica gel column, and the product isolated by flash column chromatography eluting with an ethyl acetate-heptane gradient, to afford compound 125-B as a colorless solid (2.3 g, 53%). ¹H-NMR (CDCl₃): δ 1.48 (s, 9H), 2.26 (s, 3H), 6.74 (br s, 1H), 7.21-7.26 (m, 1H), 7.31-7.36 (m, 1H), 7.54 (d, 1H), 7.71 (d, 1H); MS: m/z 264.1 (MH⁺).

(3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-carbamic acid tert-butyl ester (125-C)

Sodium hydride (60%, 0.37 g, 9.19 mmol) was added to a solution of compound 125-B (2.2 g, 8.35 mmol) in DMF (30 mL), at 0° C. and the resultant mixture was stirred for 15 minutes. 3,4-Difluorobenzylbromide (1.18 mL, 9.2 mmol) was added, and the solution was stirred at ambient temperature for 2 h. The reaction mixture was diluted with water, extracted with ethyl acetate, the organic extract washed with water (3×), brine, dried over sodium sulfate, filtered, and the solvent evaporated in vacuo. The crude residue was purified by flash column chromatography, eluting with an ethyl acetate-heptane gradient, to afford compound 125-C as an oil (2.73 g, 84%). ¹H-NMR (CDCl₃): δ 1.40 (s, 9H), 1.97 (s, 3H), 4.72 (s, 2H), 6.93-7.19 (m, 3H), 7.28-7.39 (m, 2H), 7.61 (d, 1H), 7.70 (d, 1H).

(3,4-Difluoro-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-amine (125-D)

A solution of compound 125-C (2.7 g, 6.9 mmol) in dichloromethane (40 mL) and trifluoroacetic acid (40 mL) was stirred at rt for 4 h. The solvent was evaporated in vacuo, and the residue partitioned between dichloromethane and saturated aqueous sodium bicarbonate. The organic layer was dried over sodium sulfate, and the solvent evaporated in vacuo to afford compound 125-D as a colorless solid (1.86 g, 93%). ¹H-NMR (CDCl₃): δ 2.16 (s, 3H), 4.37 (s, 2H), 7.09-7.32 (m, 5H), 7.40 (d, 1H), 7.60 (d, 1H); MS: m/z 290.1 (MH⁺).

Compound 125 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

Benzenesulfonyl chloride (0.121 mL, 0.94 mmol) was added to a solution of compound 125-D (237 mg, 0.473 mmol) and N,N-dimethylaminopyridine (catalytic amount) in pyridine (4 mL), at 0° C. The resultant solution was stirred for 30 min, allowed to warm to room temperature and stirred at ambient temperature overnight. The solvent was evaporated in vacuo, the residue partitioned between 2N HCl and dichloromethane, the layers separated, and the organic layer dried over magnesium sulfate, filtered, and the solvent evaporated in vacuo. The residue was purified by HPLC(C₁₈) eluting with an acetonitrile (0.1% TFA)-water (0.1% TFA) (40-90%) gradient to afford compound 125 as a solid (0.11 g, 54%). ¹H-NMR (CDCl₃): δ 2.04 (s, 3H), 4.64 (br s, 2H), 6.93-7.04 (m, 2H), 7.12-7.17 (m, 1H), 7.31-7.38 (m, 2H), 7.52-7.70 (m, 5H), 7.81-7.84 (m, 2H); MS: m/z 430.1 (MH⁺).

Following the procedure described above for Example 4 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 126 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-phenyl-methanesulfonamide

¹H-NMR (CDCl₃): δ 2.07 (s, 3H), 4.38 (d of d, 2H), 4.64 (d of d, 2H), 7.15-7.44 (m, 12H), 7.65 (d, 1H); MS: m/z 444.0 (MH⁺).

Compound 127 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-fluoro-benzenesulfonamide

¹H-NMR (CDCl₃) δ: 2.05 (s, 3H), 4.63 (br s, 2H), 6.94-7.07 (m, 2H), 7.10-7.18 (m, 1H), 7.33-7.40 (m, 3H), 7.50-7.69 (m, 5H); MS: m/z 448.0 (MH⁺).

Compound 128 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2-fluoro-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.50 (s, 3H), 4.88 (br s, 2H), 7.10-7.95 (m, 11H); MS: m/z 448.0 (MH⁺).

Compound 129 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-thiene-2-ylsulfonamide

¹H-NMR (DMSO-d₆): δ 2.02 (s, 3H), 4.76 (br s, 2H), 7.14-7.16 (m, 1H), 7.29-7.43 (m, 5H), 7.70 (d of d, 1H), 7.83-7.86 (m, 2H), 8.16 (d of d, 1H); MS: m/z 436.0 (MH⁺).

Compound 130 N-(Benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-1-methyl-1H-imidazole-4-sulfonamide

¹H-NMR (DMSO-d₆): δ 3.71 (s, 3H), 4.98 (s, 2H), 7.17 (s, 1H), 7.23-7.45 (m, 5H), 7.69-7.73 (m, 1H), 7.78-7.81 (m, 1H), 7.92 (s, 1H), 7.95 (s, 1H); MS: m/z 420.1 (MH⁺).

Compound 131 N-(Benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-3-fluoro-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.93 (s, 2H), 7.17-7.24 (m, 2H), 7.30-7.86 (m, 10H); MS: m/z 434.1 (MH⁺).

Compound 132 N-(Benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-4-trifluoromethyl-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.93 (s, 2H), 7.17-7.25 (m, 2H), 7.30-7.44 (m, 4H), 7.71-7.75 (m, 1H), 7.82-7.89 (m, 1H), 8.05-8.07 (m, 4H); MS: m/z 484.2 (MH⁺).

Compound 133 N-(Benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-C-methanesulfonyl-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 3.26 (m, 3H), 4.97 (s, 2H), 5.62 (s, 2H), 7.17-7.23 (m, 1H), 7.33-7.47 (m, 5H), 7.76-7.82 (m, 1H), 7.85-7.90 (m, 1H); MS: m/z 432.0 (MH⁺).

Compound 134 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.77 (s, 3H), 4.99 (s, 2H), 7.17 (s, 1H), 7.29-7.38 (m, 5H), 7.45-7.53 (m, 1H), 7.55-7.60 (t, 1H), 7.70-7.76 (m, 3H), 7.82-7.87 (m, 1H); MS: m/z 496.0 (MH⁺).

Compound 135 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.91 (s, 3H), 5.01 (s, 2H), 7.19 (s, 1H), 7.30-7.36 (m, 2H), 7.45-7.51 (t, 1H), 7.69-7.73 (m, 3H), 7.82-7.85 (m, 1H), 7.97-7.99 (d, 2H), 8.17-8.20 (d, 2H); MS: m/z 524.1 (MH⁺).

Compound 136 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.87 (s, 3H), 5.02 (s, 2H), 7.21 (s, 1H), 7.32-7.34 (m, 2H), 7.45-7.50 (t, 1H), 7.71-7.73 (m, 3H), 7.81-7.85 (m, 2H), 8.08-8.11 (m, 1H), 8.25-8.26 (m, 1H), 8.30-8.33 (s, 1H); MS: m/z 524.1 (MH⁺).

Compound 137 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.96 (s, 3H), 3.89 (s, 3H), 4.88 (s, 2H), 7.38-7.47 (m, 3H), 7.62-7.68 (m, 2H), 7.69-7.72 (m, 1H), 7.84-7.88 (m, 2H), 8.15-8.18 (m, 1H), 8.27-8.28 (m, 1H), 8.33-8.35 (m, 1H); MS: m/z 538.0 (MH⁺).

Compound 138 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.94 (s, 3H), 3.93 (s, 3H), 4.89 (s, 2H), 7.36-7.48 (m, 3H), 7.63-7.71 (m, 3H), 7.81-7.86 (m, 1H), 8.02-8.04 (m, 2H), 8.19-8.22 (m, 1H); MS: m/z 538.0 (MH⁺).

Compound 139 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.77 (s, 3H), 5.08 (s, 2H), 7.24 (s, 1H), 7.31-7.34 (m, 2H), 7.47-7.52 (m, 1H), 7.66-7.85 (m, 8H); MS: m/z 524.1 (MH⁺).

Example 5

N-(3-Bromo-benzo[b]thiophen-2-yl)-benzenesulfonamide (140-A)

Bromine (36 μL, 0.69 mmol) was added to a solution of compound 1-D (0.20 g, 0.69 mmol) in dichloromethane (10 mL) at 0° C., and stirred for 15 minutes. The resultant solution was washed with water then aqueous NaHSO₃, and dried over magnesium sulfate to afford compound 140-A as a blue solid (0.295 g). ¹H-NMR (CDCl₃): δ 6.98 (s, 1H, exchanges with D₂O), 7.25-7.44 (m, 4H), 7.49-7.54 (m, 2H), 7.64 (d of d, 1H), 7.78-7.83 (m, 2H); MS: m/z 368 (MH⁺).

Compound 140 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-benzyl)-benzenesulfonamide

Lithium bis(trimethylsilyl)amide (1.0 M in hexanes, 0.67 mL, 0.67 mmol) was added dropwise to a solution of compound 140-A (0.225 g, 0.61 mmol) in THF (3 mL) at −78° C. The solution was stirred at −78° C. for 15 minutes, to which was added a solution of 4-fluorobenzyl bromide (83 μL, 0.67 mmol) in THF (0.5 mL). The reaction mixture was allowed to warm to rt and stirred at ambient temperature for 6 days. The solution was washed with aqueous ammonium chloride, and the solvent was evaporated in vacuo. The crude residue was purified by reverse phase HPLC (C₁₈), eluting with an acetonitrile-water (0.1%) (10-90%) gradient to afford compound 140 as a colorless solid (0.130 g, 45%). ¹H-NMR (CDCl₃): δ 4.81 (s, 2H), 6.87-6.97 (m, 2H), 7.20-7.25 (m, 3H), 7.36-7.43 (m, 2H), 7.51-7.56 (m, 2H), 7.63-7.71 (m, 2H), 7.86-7.89 (m, 2H); MS: m/z 476.1 (MH⁺).

Example 6

6-Methoxy-benzo[b]thiophene-2-carboxylic acid methyl ester (141-B)

To a solution of compound 141-A (21.4 g; 139 mmol) in anhydrous DMF (165 mL) was added triethylamine (25.2 mL; 181 mmol) followed methyl thioglycolate (5.3 mL; 278 mmol) and the reaction was heated at 100° C. for 72 h. The reaction was cooled, partitioned between EtOAc and H₂O, the layers separated, the aqueous phase extracted with EtOAc, the organic extracts combined, washed with 3N NaOH, H₂O, brine, dried over Na₂SO₄, filtered, and the solvent evaporated under reduced pressure. The crude residue was triturated with CH₂Cl₂-heptanes, filtered, and the solid washed with heptanes and dried overnight to afford compound 141-B. The filtrate was evaporated and purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford a second crop of compound 141-B. The combined yield of the two crops afforded a white solid (6.55 g, 21%). ¹H-NMR (DMSO-d₆): δ 3.85 (s, 3H), 3.86 (s, 3H), 7.07-7.10 (m, 1H), 7.63 (s, 1H), 7.89-7.91 (d, 1H), 8.11 (s, 1H); MS: m/z 223.0 (MH⁺).

6-Methoxy-benzo[b]thiophene-2-carboxylic acid (141-C)

To a solution of compound 141-B (6.55 g; 29.4 mmol) in methanol (100 mL) was added 1N NaOH (44.2 mL; 44.2 mmol) and the reaction was heated at 65° C. for 18 h. The reaction was cooled, the solvent evaporated under reduced pressure, the residue dissolved in H₂O, cooled to 0° C., acidified with 2N HCl, and the solid filtered, washed with H₂O, and dried in vacuo to afford compound 141-C as a white solid (6.01 g, 98%). ¹H-NMR (DMSO-d₆): δ 3.84 (s, 3H), 7.05-7.08 (m, 1H), 7.60-7.61 (d, 1H), 7.87-7.89 (d, 1H), 8.01 (s, 1H), 13.24 (s, 1H); MS: m/z 208.9 (MH⁺).

6-Methoxy-benzo[b]thiophen-2-yl)-carbamic acid tert-butyl ester (141-D)

To a solution of compound 141-C (6.01 g; 28.8 mmol) in tert-butanol (80 mL) was added DPPA (9.30 mL; 43.2 mmol) followed by DIEA (5.51 mL; 31.6 mmol) and the reaction was refluxed for 18 h. The reaction was cooled, the solvent evaporated under reduced pressure, and the crude residue purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford compound 141-D as a beige solid (5.47 g, 68%). ¹H-NMR (DMSO-d₆): δ 1.49 (s, 9H), 3.77 (s, 3H), 6.68 (s, 1H), 6.89-6.90 (m, 1H), 7.37-7.38 (m, 1H), 7.47-7.52 (m, 1H), 10.52 (s, 1H); MS: m/z 280.0 (MH⁺).

6-(Methoxy-benzo[b]thiophen-2-yl)-amine (141-E)

To a solution of compound 141-D (4.94 g; 17.7 mmol) in EtOAc (20 mL), cooled to 0° C., was bubbled HCl_((g)), until the solution was saturated and the reaction was stirred at ambient temperature for 18 h. The solvent was evaporated under reduced pressure and the resulting residue was triturated with ether, filtered, washed with ether, and dried in vacuo to afford compound 141-E as a beige solid (3.29 g, 86%). MS: m/z 180.0 (MH⁺).

N-(6-Methoxy-benzo[b]thiophen-2-yl)-pyridin-3-yl-sulfonamide (141-F)

To a solution of compound 141-E (1.0 g; 4.63 mmol) in pyridine (15 mL), cooled to 0° C., was added 3-pyridyl sulfonyl chloride (1.49 g; 6.95 mmol) and the reaction was allowed to stir at ambient temperature for 2 h. The reaction was diluted with EtOAc, washed with 2N HCl, water, brine, dried over Na₂SO₄, filtered, the solvent evaporated under reduced pressure. The crude residue was purified by trituration of the solid with CH₂Cl₂. The solid was filtered, washed with CH₂Cl₂, and dried in vacuo to afford compound 141-F as a beige solid (1.01 g, 68%). ¹H-NMR (DMSO-d₆): δ 3.76 (s, 3H), 6.86 (s, 1H), 6.91-6.93 (m, 1H), 7.39-7.40 (d, 1H), 7.57-7.59 (d, 1H), 7.62-7.65 (m, 1H), 8.13-8.16 (m, 1H), 8.81-8.82 (m, 1H), 8.90-8.91 (d, 1H), 11.15 (s, 1H); MS: m/z 321.0 (MH⁺).

N-(3.4-Difluoro-benzyl)-N-(6-methoxy-benzo[b]thiophen-2-yl)-pyridin-3-yl-sulfonamide (141-G)

To a solution of compound 141-F (0.488 g; 1.52 mmol) in THF (15 mL) was added 1M potassium tert-butoxide (2.28 mL; 2.28 mmol) and the reaction mixture was stirred at ambient temperature for 30 min. 3,4-Difluorobenzyl bromide (0.409 g; 1.97 mmol), dissolved in THF (1.0 mL), was added drop-wise, and the reaction was stirred at ambient temperature for 18 h. The reaction was diluted with EtOAc, washed with 2N HCl, water, brine, dried over Na₂SO₄, filtered, the solvent evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford an oily semi-solid, which was further purified by reverse-phase semi-prep HPLC (Gemini, C-18 column; 100×30 mm I.D.; 5μ) eluting with a 55% to 75% MeCN—H₂O gradient to afford compound 141-G as a white solid (0.447 g, 66%). ¹H-NMR (DMSO-d₆): δ 3.76 (s, 3H), 4.89 (s, 2H), 6.93-6.96 (m, 1H), 7.11 (s, 1H), 7.19-7.20 (m, 1H), 7.34-7.43 (m, 3H), 7.60-7.62 (d, 1H), 7.70-7.73 (m, 1H), 8.21-8.24 (m, 1H), 8.93-8.96 (m, 2H); MS: m/z 447.0 (MH⁺).

Compound 141 N-(3-Bromo-6-methoxy-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-pyridin-3-yl-sulfonamide

To a solution of compound 141-G (0.044 g; 0.097 mmol) in DCE (0.5 mL) and acetic acid (0.5 mL) was added N-bromosuccinimide (0.021 g; 0.117 mmol) and the reaction was stirred at ambient temperature for 6 h. The reaction was diluted with EtOAc, washed with 10% NaHCO₃, water, brine, dried over Na₂SO₄, filtered, the solvent evaporated under reduced pressure. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) eluting with a 65% to 85% MeCN—H₂O gradient to afford compound 141 as a beige solid (0.014 g, 28%). ¹H-NMR (DMSO-d₆): δ 3.80 (s, 3H), 4.86 (s, 2H), 7.08-7.16 (m, 2H), 7.32-7.40 (m, 2H), 7.54-7.57 (m, 2H), 7.72-7.75 (m, 1H), 8.29-8.32 (m, 1H), 8.91-8.97 (d, 1H), 9.00-9.05 (m, 1H); MS: m/z 525 (MH⁺).

Following the procedure described above for Example 6 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 142 N-(3,4-Difluoro-benzyl)-N-(7-methoxy-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.88 (s, 3H), 4.88 (s, 2H), 6.87-6.91 (m, 1H), 7.14-7.41 (m, 6H), 7.63-7.79 (m, 2H), 7.80-7.91 (m, 3H); MS: m/z 446.1 (MH⁺).

Compound 375 N-(6-Fluoro-3-methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carbomethoxy-benzenesulfonamide

MS: m/z 555.9 (MH⁺).

Compound 412 N-(6-Fluoro-3-methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-carbomethoxybenzenesulfonamide

MS: m/z 489.9 (MH⁺).

Example 7

Compound 143 N-(3-Chloro-7-methoxy-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-benzenesulfonamide

To a solution of compound 142 (0.061 g; 0.137 mmol) in DCE (0.5 mL) and acetic acid (0.5 mL) was added N-chlorosuccinimide (0.027 g; 0.206 mmol) and the reaction was stirred at ambient temperature for 2 h. The reaction was diluted with EtOAc, washed with 10% NaHCO₃, water, brine, dried over Na₂SO₄, filtered, the solvent evaporated under reduced pressure. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) eluting with a 60% to 80% MeCN—H₂O gradient to afford compound 143 as a beige solid (0.011 g, 17%). ¹H-NMR (CD₃OD): δ 3.94 (s, 3H), 4.80 (s, 2H), 6.96-7.23 (m, 5H), 7.27-7.41 (m, 1H), 7.60-7.65 (m, 2H), 7.72-7.76 (m, 1H), 7.87-7.90 (m, 2H); MS: m/z 480.0 (MH⁺).

Compound 144 N-(3,6-Dichloro-7-methoxy-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-benzenesulfonamide

¹H-NMR (CD₃OD): δ 3.94 (s, 3H), 4.83 (s, 2H), 6.90-6.92 (m, 1H), 7.03-7.18 (m, 2H), 7.21-7.23 (m, 1H), 7.34-7.36 (m, 1H), 7.61-7.65 (m, 2H), 7.73-7.77 (m, 1H), 7.82-7.90 (m, 2H); MS: m/z 513.9 (MH⁺).

Example 8

3-Chloro-pyridine 1-oxide (145-B)

To a solution of 3-chloropyridine, (22.71 g, 200 mmol) in acetic acid (80 mL) was added hydrogen peroxide solution (30% aqueous, 40 mL), and the mixture was heated at 80° C. for 15 h. Additional hydrogen peroxide solution (30% aqueous, 5 mL) was added to the reaction mixture and the heating continued an additional 5 h. After cooling, the reaction mixture was quenched into a solution of NaHSO₃ in water (400 mL), using starch-iodine paper to confirm the destruction of excess hydrogen peroxide. The mixture was evaporated in vacuo and partitioned between water (100 mL) and dichloromethane (250 mL). The organics were washed with saturated NaHCO₃ solution (2×100 mL), and brine (100 mL). The combined aqueous layers were extracted with dichloromethane (8×100 mL), the organic extracts were combined, dried over Na₂SO₄, filtered, and evaporated in vacuo. The organic residue was partitioned between dichloromethane/water, treated with solid NaHCO₃, and filtered. The aqueous washes from the first extraction were treated with NaHCO₃, extracted with dichloromethane (3×100 mL), and the combined organics dried with Na₂SO₄, filtered, and evaporated in vacuo to afford compound 145-B as an orange oil (22.37 g, 86%). ¹H-NMR (DMSO-d₆): δ 7.40-7.53 (m, 2H), 8.22 (d, 1H), 8.52 (s, 1H); MS: m/z 130.1 (MH⁺).

3-Chloro-pyridine-2-carbonitrile (145-C)

To a solution of compound 145-B, (22.37 g, 172.7 mmol) in acetonitrile (175 mL) was added triethylamine (48 mL, 346 mmol) and TMS-CN (56 mL, 420 mmol). The solution was heated at reflux for 20 h then evaporated in vacuo. The residue was partitioned between EtOAc (250 mL), 10% aqueous Na₂CO₃ (50 mL), and filtered over celite. The organic portion of the filtrate was washed with 10% aqueous Na₂CO₃ (2×50 mL), brine (50 mL), and the organics dried over Na₂SO₄, filtered, and evaporated in vacuo to afford a dark crystalline residue, which was dissolved in warm diethyl ether (200 mL), filtered, and evaporated in vacuo to afford compound 145-C as a tan-orange powder (23.41 g, 98%). ¹H-NMR (DMSO-d₆): δ 7.78-7.84 (m, 1H), 8.30 (d, 1H), 8.73 (d, 1H); MS: m/z 139.1 (MH⁺).

3-Amino-thieno[3,2-b]pyridine-2-carboxylic acid methyl ester (145-D)

To a solution of compound 145-C (23.41 g, 169.0 mmol) in acetonitrile (170 mL) was added methyl thioglycolate (16.2 mL, 178 mmol) and K₂CO₃ (46.72 g, 338 mmol). The mixture was heated under reflux for 3 h then filtered hot and the filter cake rinsed with acetonitrile. The filter cake was suspended in refluxing acetonitrile, filtered hot, and rinsed with additional acetonitrile. The combined filtrates were evaporated in vacuo, the residue triturated with warm water (250 mL), filtered, and rinsed with water. The solid was dissolved in warm methanol (500 mL), treated with charcoal, filtered, and evaporated in vacuo. The residue was triturated with ethanol (25 mL), filtered, washed with ethanol (25 mL), and dried in vacuo to afford compound 145-D as a brown powder (21.65 g, 62%). ¹H-NMR (DMSO-d₆): δ 3.83 (s, 3H), 6.91 (s, 2H), 7.52-7.59 (m, 1H), 8.40 (dd, 1H), 8.69 (dd, 1H); MS: m/z 209.1 (MH⁺).

3-Bromo-thieno[3,2-b]pyridine-2-carboxylic acid methyl ester (145-E)

To a solution of CuBr (15.09 g, 105.2 mmol) in 48% aqueous HBr (250 mL), cooled in an ice bath, was added compound 145-D (20.82 g, 100 mmol). To the reaction mixture was added a solution of NaNO₂ (8.29 g, 120 mmol) in water (200 mL) drop-wise over 1 h. After 30 min, solid NaNO₂ (0.83 g, 12.0 mmol) was added, and after another 30 min an additional portion of solid NaNO₂ (0.83 g, 12.0 mmol) was added. After 10 min the reaction mixture was carefully poured into a mixture of ice (1 L) and NaHCO₃ (200 g). The mixture was extracted with dichloromethane (5×200 mL), and the combined organic extracts dried over MgSO₄, filtered, and evaporated in vacuo to afford compound 145-E as a brown powder (25.16 g). ¹H-NMR (DMSO-d₆): δ 3.94 (s, 3H), 7.65 (m, 1H), 8.65 (dd, 1H), 8.88 (dd, 1H); MS: m/z 272.0 (MH⁺).

3-Bromo-thieno[3,2-b]pyridine-2-carboxylic acid (145-F)

To a solution of compound 145-E (4.94 g, 18.2 mmol) in 5:1 THF/H₂O (200 mL) was added LiOH.H₂O (0.797 g, 19.0 mmol). The reaction was stirred for 3 days then concentrated in vacuo, to which was added water (100 mL) and 1N HCl (19.0 mL), and the resultant precipitate was isolated by filtration. The solid was rinsed with water and dried under vacuum to afford compound 145-F as a tan-yellow solid (4.51 g, 96%). ¹H-NMR (DMSO-d₆): δ 7.62 (dd, 1H), 8.62 (dd, 1H), 8.86 (dd, 1H), 14.18 (br s, 1H); MS: m/z 257.9 (MH⁺).

3-Bromo-thieno[3,2-b]pyridin-2-yl)-carbamic acid tert-butyl ester (145-G)

A solution of compound 145-F (2.0 g, 7.75 mmol), N,N-diisopropylethylamine (1.49 mL, 8.52 mmol) and diphenyl phosphoryl azide (2.07 mL, 9.30 mmol) in t-butanol (20 mL) was heated at reflux for 16 h. The solvent was evaporated in vacuo, the residue dissolved in dichloromethane, washed with 1N NaOH, brine, dried with Na₂SO₄, and evaporated to afford a crude residue which was purified by flash column chromatography (SiO₂), eluting with dichloromethane to afford compound 145-G as a yellow solid (1.51 g, 56%). ¹H-NMR (CDCl₃): δ 1.6 (s, 9H), 7.2 (d of d, 1H), 7.5 (br s, 1H), 8.0 (d, 1H), 8.7 (d, 1H); MS: m/z 251 (MH⁺).

3-Bromo-thieno[3,2-b]pyridin-2-ylamine hydrochloride (145-H)

Compound 145-G (0.75 g, 2.28 mmol) was added to a solution of HCl in dioxane (4 N, 7.5 mL) and the reaction mixture was stirred at rt for 2 h. The solvent was evaporated under reduced pressure to afford compound 145-H as a yellow solid (0.74 g). ¹H-NMR (DMSO-d₆): δ 7.3 (d, 1H), 8.3 (d, 1H), 8.5 (br s, 2H) superimposed on 8.55 (d, 1H).

N-(3-Bromo-thieno[3,2-b]pyridin-2-yl)-benzenesulfonamide hydrochloride (145-I)

To a solution of compound 145-H (0.46 g, 1.52 mmol) in pyridine (4.6 mL), cooled to 0° C., was added benzenesulfonyl chloride (0.206 mL, 1.60 mmol), and the reaction was heated to 50° C. for 72 h. Additional benzenesulfonyl chloride (0.412 mL, 3.20 mmol) was added and the reaction mixture was heated at 50° C. for an additional 16 h. The solvent was evaporated in vacuo, the residue dissolved in dichloromethane and washed with aqueous sodium bicarbonate. The aqueous layer was acidified with 1N HCl, extracted with dichloromethane, and the organic layer was evaporated in vacuo to afford a yellow solid (0.22 g, 36%) as a 1/3.5 mixture of the 3-bromo- and 3-chloro-substituted compounds, 145-Ia and 145-Ib, respectively. ¹H-NMR (DMSO-d₆): δ 7.1-7.2 (m, 1H), 7.4-7.6 (m, 3H), 7.8 (m, 2H), 8.1-8.2 (m, 1H), 8.25-8.35 (m, 1H); MS: m/z 465 and 509 (MH⁺).

Compound 145 N-(3-Bromo-thieno[3,2-b]pyridin-2-yl)-N-(3,4-difluoro-benzyl)-benzenesulfonamide and N-(3-chloro-thieno[3,2-b]pyridin-2-yl)-N-(3,4-difluoro-benzyl)-benzenesulfonamide

To a mixture of compounds 145-Ia and 145-Ib (90 mg, 0.222 mmol) in DMF (1 mL), at rt, was added 1.0M sodium bis(trimethylsilyl)amide in THF (0.44 mL, 0.444 mmol). The solution was stirred 30 min at rt to which was added 3,4-difluorobenzyl bromide (0.029 mL, 0.222 mmol). The resultant solution was stirred at ambient temperature for 16 h, to which was added additional DMF (1 mL) followed by 3,4-difluorobenzyl bromide (0.029 mL, 0.222 mmol), and the reaction mixture stirred at rt for 3 days. The solvent was evaporated and the residue purified by reverse-phase HPLC eluting with an acetonitrile-water gradient. Further purification by flash column chromatography (SiO₂), eluting with dichloromethane, afforded compound 145 as a clear, hard gum (19.7 mg, 18%). ¹H-NMR (DMSO-d₆): δ 4.74 (s, 2H), 7.00-7.10 (s superimposed on m, 3H), 7.15-7.21 (m, 1H), 7.26-7.36 (m, 2H), 7.49-7.54 (m, 2H), 7.62-7.67 (m, 3H), 7.73-7.78 (m, 2H); MS: m/z 416.1 (MH⁺).

Example 9

Thieno[3,2-b]pyridin-2-ylamine hydrochloride (146-A)

A mixture of compound 145-H, (1.86 g, 6.16 mmol) and 10% Pd/C (0.49 g, 26.3% w/w) in methanol (75 mL) was catalytically hydrogenated on a Parr shaker at 25 psi. After 3 h, the catalyst was filtered, the reaction mixture recharged with 10% Pd/C (0.49 g, 26.3% w/w) and shaken an additional 16 h at 22 psi H₂. The reaction was filtered, recharged with 10% Pd/C (0.20 g, 10.8% w/w), and shaken at 20 psi H₂ for an additional 24 h. The reaction mixture was filtered, evaporated, and the free base isolated by washing with aqueous sodium bicarbonate. The resultant residue was purified by flash column chromatography (SiO₂), eluting with 3% MeOH/CH₂Cl₂ to afford compound 146-A as a yellow solid (0.65 g, 57%). ¹H-NMR (DMSO-d₆): δ 6.4 (s, 1H), 7.1 (dd, 1H), 8.3 (2, 1H), 8.4 (s, 2H), 8.5 (d, 1H), 15.2 (br s, 1H); MS: m/z 151.1 (MH⁺).

N-Thieno[3,2-b]pyridin-2-yl-benzenesulfonamide hydrochloride (146-B)

To a suspension of compound 146-A (0.65 g, 2.91 mmol) in pyridine (30 mL), at rt, was added benzenesulfonyl chloride (0.751 mL, 5.83 mmol), and the reaction was stirred for 16 h. Additional benzenesulfonyl chloride (0.225 mL, 1.76 mmol) was added and the reaction mixture was stirred at rt for an additional 16 h. The solvent was evaporated in vacuo, the residue treated with 1N HCl and extracted several times with dichloromethane and ethyl acetate. The aqueous layer was filtered, dissolved in methanol, and the combined organic extracts were evaporated in vacuo. The resultant residue was purified by reverse phase HPLC, eluting with an MeCN—H₂O gradient to afford compound 146-B as an orange solid (0.24 g, 20%). ¹H-NMR (CD₃CN): δ 6.92 (s, 1H), 7.2 8.0 (d of d, 1H), 7.46 (m, 2H), 7.56 (m, 1H), 7.85 (m, 2H), 8.27 (d, 1H), 8.35 (d, 1H); MS: m/z 291.09 (MH⁺).

Compound 146 N-(3,4-Difluoro-benzyl)-N-thieno[3,2-b]pyridin-2-yl-benzenesulfonamide

To compound 146-B, (0.237 g, 0.725 mmol) in DMF (1 mL), cooled to 0° C., was added 1.0M potassium t-butoxide in THF (1.71 mL, 1.71 mmol), drop-wise over 5 min. The solution was stirred for 30 min at 0° C., to which was added 4-fluoro-3-trifluoromethylbenzyl bromide (0.132 mL, 0.898 mmol). The resultant solution was stirred 5 min at 0° C. and allowed to warm to rt and stirred overnight. Saturated sodium bicarbonate solution was added, and the mixture evaporated in vacuo. The residue was partitioned between water and diethyl ether, the organic phase separated, and the aqueous phase extracted with diethyl ether. The combined organic phases were evaporated in vacuo and the crude residue purified by reverse-phase HPLC to afford compound 146 as a dark solid (28 mg, 8%). ¹H-NMR (CDCl₃): δ 5.00 (s, 2H), 7.16 (t, 1H), 7.44 (d of d, 1H), 7.56 (m, 3H), 7.69 (m, 3H), 7.85 (m, 1H), 8.33 (d, 2H), 8.57 (d, 1H); MS: m/z 467.09 (MH⁺).

Example 10

Thieno[2,3-b]pyridine-2-carboxylic acid methyl ester (147-B)

To 2-chloro-3-pyridine carboxaldehyde, compound 147-A, (5.07 g, 35.8 mmol), dissolved in MeCN (30 mL) was added triethylamine (6.5 mL, 46.5 mmol) followed by methyl thioglycolate (3.49 mL, 38.3 mmol) and the reaction was refluxed for 18 h. The reaction mixture was cooled and the solvent evaporated under reduced pressure. The crude residue was partitioned between H₂O and EtOAc, the layers separated and the aqueous phase extracted with EtOAc. The organic layers were combined, washed with H₂O, brine, dried over Na₂SO₄, filtered, and the solvent evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford compound 147-B as a white solid (2.01 g, 29%). ¹H-NMR (DMSO-d₆): δ 3.91 (s, 3H), 7.54-7.57 (m, 1H), 8.23 (s, 1H), 8.43-8.46 (m, 1H), 8.72-8.74 (m, 1H); MS: m/z 194.1 (MH⁺).

Thieno[2,3-b]pyridine-2-carboxylic acid (147-C)

To a solution of compound 147-B (0.508 g, 2.63 mmol) in a mixture of MeOH (15 mL) and H₂O (3 mL) was added 3N NaOH (1.9 mL, 5.66 mmol) and the reaction mixture was stirred at ambient temperature for 5 h. The solvent was evaporated under reduced pressure, the residue dissolved in H₂O, and acidified with 1N HCl. The precipitate was filtered, washed with H₂O, and dried under vacuum to afford compound 147-C as a white solid (0.366 g, 78%). MS: m/z 180.0 (MH⁺).

Thieno[2,3-b]pyridin-2-yl-carbamic acid tert-butyl ester (147-D)

A solution of compound 147-C (0.36 g, 2.00 mmol), N,N-diisopropylethylamine (0.385 mL, 2.21 mmol) and diphenyl phosphoryl azide (0.536 mL, 2.41 mmol) in t-butanol (3.6 mL) was heated at reflux for 16 h. The solvent was evaporated in vacuo, the residue dissolved in dichloromethane, washed with 1 N NaOH, brine, dried with Na₂SO₄, filtered, and evaporated to afford a residue. Flash column chromatography (SiO₂) eluting with dichloromethane afforded compound 147-D as a white solid (0.25 g, 50%). ¹H-NMR (CDCl₃): δ 1.55 (s, 9H), 6.60 (s, 1H), 7.20 (dd, 1H), 7.80 (d, 1H), 8.40 (d, 1H); MS: m/z 251.2 (MH⁺).

Thieno[2,3-b]pyridin-2-ylamine dihydrochloride (147-E)

Compound 147-D (3.76 g, 15.0 mmol) was added to a solution of HCl in dioxane (4 N, 40 mL). The mixture was stirred at rt for 3 days and the solid filtered to afford compound 147-E as a yellow solid (3.24 g, 97%). ¹H-NMR (DMSO-d₆): δ 6.12 (s, 1H), 7.50 (dd, 1H), 8.02 (d, 1H), 8.28 (d, 1H), 9.60 (br s, 3H).

N-Thieno[2,3-b]pyridin-2-yl-benzenesulfonamide (147-F)

Compound 147-E (0.22 g, 1.00 mmol) in pyridine (5.0 mL) was stirred at rt for 30 min, to which was added benzenesulfonyl chloride (0.135 mL, 1.05 mmol) and the reaction mixture was stirred at rt for 4 h. Another portion of benzenesulfonyl chloride (0.030 mL, 0.235 mmol) was added and the reaction mixture stirred at rt for 72 h. Water and saturated sodium bicarbonate solution were added and the mixture was extracted with dichloromethane, dried over sodium sulfate and evaporated in vacuo to afford a residue. Flash column chromatography (SiO₂) eluting with dichloromethane afforded compound 147-F as a yellow solid (0.24 g, 83%).

Compound 147 N-(3,4-Difluoro-benzyl)-N-thieno[2,3-b]pyridin-2-yl-benzenesulfonamide

To compound 147-F (0.24 g, 0.827 mmol) in DMF (2.5 mL) at rt was added 1.0 M lithium bis(trimethylsilyl)amide in THF (0.87 mL, 0.87 mmol), drop-wise, and the solution was stirred 5 min. 3,4-Difluorobenzyl bromide (0.114 mL, 0.868 mmol) was added to the reaction mixture and the resultant solution was stirred at ambient temperature overnight. Additional amounts of 1.0 M lithium bis(trimethylsilyl)amide in THF (0.44 mL, 0.44 mmol) and 3,4-difluorobenzyl bromide (0.052 mL, 0.406 mmol) were added and stirred for 18 h. Saturated sodium bicarbonate solution was added, the mixture evaporated in vacuo, and the residue partitioned between water and diethyl ether and evaporated in vacuo to afford a residue Purification by reverse-phase HPLC eluting with an acetonitrile-water (0.1% TFA) gradient afforded a brownish gum that was dissolved in acetonitrile, and converted to its hydrochloride salt by the addition of ethereal hydrogen chloride. The solid was filtered, washed with diethyl ether, and dried under vacuum to afford compound 147 as a tan solid (32.3 mg, 9%). ¹H-NMR (DMSO-d₆): δ 4.95 (s, 2H), 7.20 (s, 1H), 7.25 (m, 1H), 7.40 (m, 3H), 7.70 (t, 2H), 7.80 (t, 1H), 7.90 (d, 2H), 8.20 (d, 2H), 8.30 (d, 2H), 12.4 (br s, 1H); MS: m/z 417.16 (MH⁺).

Example 11

Compound 148 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-benzenesulfonamide

To a solution of compound 1 (440 mg, 1.06 mmol) in 1,2-dichloroethane (3 mL) and acetic acid (3 mL), at 0° C., was added N-bromosuccinimide (207 mg, 1.16 mmol), and the reaction mixture was stirred at rt for 1 h. The solvent was evaporated in vacuo, and the residue partitioned between dichloromethane and a saturated solution of aqueous sodium bicarbonate. The organic layer was separated, the product pre-absorbed onto silica gel, and purified by flash column chromatography eluting with an ethyl acetate-heptane gradient (5-50%) to afford compound 148 as a colorless solid (190 mg, 36%). ¹H-NMR (DMSO-d₆): δ 4.82 (s, 2H), 7.11-7.14 (m, 1H), 7.28-7.39 (m, 2H), 7.46-7.58 (m, 2H), 7.67-7.72 (m, 3H), 7.80-7.85 (m, 1H), 7.91-7.97 (m, 3H); MS: m/z 494.1 (MH⁺).

Following the procedure described above for example 11 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 149 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-pyridin-3-yl-sulfonamide

¹H-NMR (DMSO-d₆): δ 4.89 (s, 2H), 7.12-7.19 (m, 1H), 7.32-7.42 (m, 2H), 7.48-7.55 (m, 2H), 7.66-7.77 (m, 2H), 7.94-8.00 (m, 1H), 8.30-8.35 (m, 1H), 8.98 (dd, 1H), 9.06 (d, 1H); MS: m/z 495 (MH⁺).

Compound 150 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-1-methyl-1H-imidazole-4-sulfonamide

¹H-NMR (DMSO-d₆): δ 3.75 (s, 3H), 4.87 (s, 2H), 7.11-7.19 (m, 1H), 7.28-7.52 (m, 4H), 7.66-7.72 (m, 1H), 7.90-7.96 (m, 2H), 8.01 (s, 1H); MS: m/z 498 (MH⁺).

Compound 151 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 3.39 (s, 3H), 4.87 (s, 2H), 7.15-7.21 (m, 1H), 7.32-7.54 (m, 4H), 7.70-7.76 (m, 1H), 7.95-8.01 (m, 1H); MS: m/z 432.0 (MH⁺).

Compound 152 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.39 (t, 3H), 3.51 (q, 2H), 4.88 (s, 2H), 7.12-7.18 (m, 1H), 7.32-7.42 (m, 2H), 7.49-7.54 (m, 2H), 7.71-7.76 (m, 1H), 7.94-7.99 (m, 1H); MS: m/z 446 (MH⁺).

Compound 153 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-propane-1-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.04 (t, 3H), 1.79-1.93 (m, 2H), 3.45-3.51 (m, 2H), 4.87 (s, 2H), 7.12-7.18 (m, 1H), 7.31-7.43 (m, 2H), 7.48-7.55 (m, 2H), 7.70-7.76 (m, 1H), 7.94-7.99 (m, 1H); MS: m/z 460 (MH⁺).

Compound 154 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-butane-1-sulfonamide

¹H-NMR (DMSO-d₆): δ 0.92 (t, 3H), 1.38-1.53 (m, 2H), 1.74-1.86 (m, 2H), 3.45-3.53 (m, 2H), 4.88 (s, 2H), 7.12-7.18 (m, 1H), 7.32-7.43 (m, 2H), 7.48-7.54 (m, 2H), 7.70-7.76 (m, 1H), 7.94-8.00 (m, 1H); MS: m/z 474.1 (MH⁺).

Compound 155 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-3-fluoro-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.87 (br s, 2H), 7.10-7.17 (m, 1H), 7.30-7.41 (m, 2H), 7.47-7.54 (m, 2H), 7.67-7.83 (m, 5H), 7.94-8.01 (m, 1H); MS: m/z 512 (MH⁺).

Compound 156 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-4-trifluoromethyl-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.88 (s, 2H), 7.12-7.18 (m, 1H), 7.30-7.41 (m, 2H), 7.48-7.54 (m, 2H), 7.67-7.73 (m, 1H), 7.96-8.01 (m, 1H), 8.08 (d, 2H), 8.15 (d, 2H); MS: m/z 562 (MH⁺).

Compound 157 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 3.40 (s, 3H), 4.96 (s, 2H), 7.43-7.55 (m, 3H), 7.68-7.80 (m, 3H), 7.97-8.02 (m, 1H); MS: m/z 482.1 (MH⁺).

Compound 158 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-chloro-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.79 (s, 2H), 7.21 (s, 4H), 7.38-7.41 (m, 2H) 7.51-7.56 (m, 2H), 7.61-7.72 (m, 3H), 7.85-7.87 (m, 2H); MS: m/z 447.9 (MH⁺).

Compound 159 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-chloro-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.81 (s, 2H), 7.21 (s, 4H), 7.38-7.41 (m, 2H) 7.51-7.56 (m, 2H), 7.63-7.71 (m, 3H), 7.85-7.87 (m, 2H); MS: m/z 492.0 (MH⁺).

Compound 160 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.55 (s, 3H), 4.93 (s, 2H), 6.68-6.70 (d, 1H), 6.79-6.83 (t, 1H), 7.16-7.20 (m, 1H), 7.30-7.32 (m, 1H), 7.35-7.38 (m, 2H), 7.48-7.52 (m, 2H), 7.59-7.63 (m, 2H), 7.68-7.71 (m, 1H), 7.86-7.89 (m, 2H); MS: m/z 487.9 (MH⁺).

Compound 161 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5-bromo-2-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.52 (s, 3H), 4.88 (s, 2H), 6.55-6.59 (d, 1H), 7.26-7.29 (m, 1H), 7.38-7.40 (m, 2H), 7.49-7.53 (m, 3H), 7.61-7.66 (m, 2H), 7.70-7.73 (m, 1H), 7.86-7.88 (m, 2H); MS: m/z 567.9 (MH⁺).

Compound 162 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.72 (s, 3H), 4.82 (s, 2H), 6.74-6.87 (m, 3H), 7.09-7.14 (t, 1H), 7.36-7.40 (m, 2H), 7.51-7.56 (m, 2H), 7.62-7.71 (m, 3H), 7.86-7.89 (m, 2H); MS: m/z 488.0 (MH⁺).

Compound 163 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-bromo-5-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.75 (s, 3H), 5.02 (s, 2H), 6.63-6.68 (m, 1H), 7.21-7.22 (m, 1H), 7.26-7.29 (m, 1H), 7.38-7.41 (m, 2H), 7.51-7.55 (m, 2H), 7.63-7.72 (m, 3H), 7.87-7.90 (m, 2H); MS: m/z 567.9, (MH⁺), 589.8 (MNa⁺).

Compound 164 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.73 (s, 3H), 4.79 (s, 2H), 6.70-6.74 (m, 2H), 7.15-7.18 (m, 2H), 7.34-7.39 (m, 2H), 7.51-7.55 (m, 2H), 7.61-7.72 (m, 3H), 7.86-7.88 (m, 2H); MS: m/z 488.0 (MH⁺), 510.0 (MNa⁺).

Compound 165 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3-bromo-4-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.82 (s, 3H), 4.75 (s, 2H), 6.71-6.73 (d, 1H), 7.15-7.18 (m, 1H), 7.38-7.46 (m, 3H), 7.52-7.57 (m, 2H), 7.64-7.72 (m, 3H), 7.86-7.78 (m, 2H); MS: m/z 567.9 (MH⁺), 589.8 (MNa⁺).

Compound 166 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-fluoro-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.93 (s, 2H), 6.88-6.93 (t, 1H), 7.02-7.07 (t, 1H), 7.18-7.22 (m, 1H), 7.36-7.47 (m, 3H), 7.49-7.55 (m, 2H), 7.62-7.73 (m, 3H), 7.87-7.90 (d, 2H); MS: m/z 475.9 (MH⁺).

Compound 167 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3-nitro-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.94 (s, 2H), 7.39-7.49 (m, 3H), 7.51-7.58 (m, 2H), 7.64-7.76 (m, 4H), 7.88-7.89 (d, 2H), 8.10-8.12 (m, 2H); MS: m/z 524.8 (MH⁺).

Compound 168 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(pyridin-2-ylmethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 5.08 (s, 2H), 7.27-7.31 (m, 1H), 7.37-7.41 (m, 2H), 7.51-7.55 (m, 2H), 7.64-7.74 (m, 3H), 7.80-7.88 (m, 4H), 8.47-8.49 (d, 1H); MS: m/z 459.0 (MH⁺).

Compound 169 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(pyridin-3-ylmethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.86 (s, 2H), 7.27-7.30 (m, 1H), 7.38-7.42 (m, 2H), 7.51-7.57 (m, 2H), 7.62-7.71 (m, 3H), 7.83-7.91 (m, 3H), 8.41-8.42 (m, 1H), 8.51-8.42 (m, 1H); MS: m/z 459.0 (MH⁺).

Compound 170 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(pyridin-4-ylmethyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 5.07 (s, 2H), 7.44-7.47 (m, 2H), 7.53-7.59 (m, 2H), 7.68-7.73 (m, 3H), 7.83-7.91 (m, 4H), 8.81-8.83 (m, 2H); MS: m/z 459.0, 461.0 (MH⁺).

Compound 171 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-nitro-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 5.33 (s, 2H), 7.38-7.46 (m, 3H), 7.52-7.57 (m, 2H), 7.65-7.70 (m, 4H), 7.82-7.86 (m, 2H), 7.92-7.96 (d, 1H), 8.06-8.08 (d, 1H); MS: m/z 502.9, 504.9 (MH⁺).

Compound 172 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-trifluoromethoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 5.00 (s, 2H), 7.10-7.14 (m, 1H), 7.23-7.28 (m, 2H), 7.35-7.42 (m, 2H), 7.50-7.56 (m, 2H), 7.62-7.71 (m, 4H), 7.76-7.78 (m, 2H); MS: m/z 541.9, 543.9 (MH⁺).

Compound 173 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3-trifluoromethoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.85 (s, 2H), 7.07-7.09 (m, 1H), 7.14 (s, 1H), 7.21-7.27 (m, 2H), 7.37-7.42 (m, 2H), 7.51-7.55 (m, 2H), 7.62-7.72 (m, 3H), 7.86-7.89 (m, 2H); MS: m/z 542.0, 543.9 (MH⁺).

Compound 174 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.85 (s, 2H), 7.07-7.08 (d, 2H), 7.30-7.32 (m, 2H), 7.37-7.42 (m, 2H), 7.51-7.55 (d, 2H), 7.62-7.72 (m, 3H), 7.85-7.87 (m, 2H); MS: m/z 542.0 (MH⁺).

Compound 175 N-(Benzyl)-N-(3-bromo-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.85 (s, 2H), 7.20-7.29 (m, 5H), 7.35-7.40 (m, 2H), 7.51-7.55 (m, 2H), 7.61-7.70 (m, 3H), 7.87-7.89 (d, 2H); MS: m/z 458.0, 460.0 (MH⁺).

Compound 176 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-methoxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 3.79 (s, 3H), 4.79 (s, 2H), 6.65-6.70 (m, 1H), 6.84-6.89 (m, 1H), 6.98-6.99 (m, 1H), 7.36-7.42 (m, 2H), 7.52-7.55 (m, 2H), 7.63-7.72 (m, 3H), 7.86-7.89 (d, 2H); MS: m/z 506.0 (MH⁺).

Compound 177 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.84 (s, 2H), 7.04-7.09 (m, 1H), 7.39-7.44 (m, 2H), 7.47-7.57 (m, 4H), 7.65-7.73 (m, 3H), 7.85-7.88 (m, 2H); MS: m/z 544.0 (MH⁺).

Compound 178 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-methyl-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.40 (s, 3H), 4.89 (s, 2H), 6.92-6.95 (m, 1H), 7.07-7.09 (m, 3H), 7.35-7.39 (m, 2H), 7.51-7.55 (m, 2H), 7.59-7.68 (m, 3H), 7.87-7.90 (d, 2H); MS: m/z 472.0 (MH⁺).

Compound 179 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3-methyl-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.23 (s, 3H), 4.82 (s, 2H), 6.99-7.11 (m, 4H), 7.35-7.39 (m, 2H), 7.49-7.57 (m, 2H), 7.61-7.72 (m, 3H), 7.86-7.88 (d, 2H); MS: m/z 472.0 (MH⁺).

Compound 180 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-methoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.89 (s, 3H), 4.87 (s, 2H), 7.17-7.21 (d, 2H), 7.40-7.47 (m, 1H), 7.49-7.53 (m, 2H), 7.62-7.73 (m, 3H), 7.83-7.87 (d, 2H), 7.94-8.00 (m, 1H); MS: m/z 530.0 (MH⁺).

Compound 181 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.84 (s, 3H), 4.90 (s, 2H), 7.38-7.54 (m, 6H), 7.58-7.75 (m, 4H), 7.97-8.01 (m, 1H); MS: m/z 530.0 (MH⁺).

Compound 182 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.89 (s, 3H), 4.86 (s, 2H), 7.18-7.22 (d, 2H), 7.39-7.52 (m, 3H), 7.61-7.71 (m, 3H), 7.83-7.87 (d, 2H), 7.95-7.99 (m, 1H); MS: m/z 574.0 (MH⁺).

Compound 183 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.36-1.41 (t, 3H), 3.50-3.57 (q, 2H), 4.96 (s, 2H), 7.43-7.54 (m, 3H), 7.66-7.76 (m, 3H), 7.96-7.99 (m, 1H); MS: m/z 495.9 (MH⁺).

Compound 184 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-thiophene-2-sulfonamide

¹H-NMR (DMSO-d₆): δ 4.93 (s, 2H), 7.34-7.38 (m, 1H), 7.41-7.47 (m, 1H), 7.48-7.53 (m, 2H), 7.65-7.72 (m, 3H), 7.90-7.91 (m, 1H), 7.98-8.02 (m, 1H), 8.19-8.21 (m, 1H); MS: m/z 549.9 (MH⁺).

Compound 185 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-methoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.64 (s, 3H), 4.91 (s, 2H), 7.37-7.53 (m, 6H), 7.59-7.72 (m, 4H), 7.97-7.99 (m, 1H); MS: m/z 574.0 (MH⁺).

Compound 186 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-thien-3-yl-sulfonamide

¹H-NMR (DMSO-d₆): δ 4.92 (s, 2H), 7.41-7.54 (m, 4H), 7.64-7.71 (m, 3H), 7.91-7.99 (m, 2H), 8.46-8.47 (m, 1H); MS: m/z 549.9 (MH⁺).

Compound 187 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-thien-3-yl-sulfonamide

¹H-NMR (DMSO-d₆): δ 4.93 (s, 2H), 7.42-7.56 (m, 4H), 7.64-7.76 (m, 3H), 7.91-8.00 (m, 2H), 8.46-8.47 (m, 1H); MS: m/z 506.0 (MH⁺).

Compound 188 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-pyridin-3-yl-sulfonamide

¹H-NMR (DMSO-d₆): δ 4.99 (s, 2H), 7.43-7.53 (m, 3H), 7.67-7.76 (m, 4H), 7.96-8.02 (m, 1H), 8.32-8.36 (m, 1H), 8.98-9.01 (m, 1H), 9.08-9.09 (m, 1H); MS: m/z 545.0 (MH⁺).

Compound 189 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-pyridin-3-yl-sulfonamide

¹H-NMR (DMSO-d₆): δ 5.01 (s, 2H), 7.43-7.53 (m, 3H), 7.67-7.76 (m, 4H), 7.98-8.03 (m, 1H), 8.32-8.36 (m, 1H), 8.97-9.02 (m, 1H), 9.06-9.09 (m, 1H); MS: m/z 501.0 (MH⁺).

Compound 190 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.22-1.44 (t, 3H), 3.49-3.57 (q, 2H), 4.97 (s, 2H), 7.44-7.54 (m, 3H), 7.67-7.79 (m, 3H), 7.96-8.03 (m, 1H); MS: m/z 452.0 (MH⁺).

Compound 191 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-thiophene-2-sulfonamide

¹H-NMR (DMSO-d₆): δ 4.93 (s, 2H), 7.34-7.36 (m, 2H), 7.43-7.57 (m, 3H), 7.66-7.76 (m, 2H), 7.89-7.92 (m, 1H), 7.97-8.03 (m, 1H), 8.19-8.23 (m, 1H); MS: m/z 528.0 (MH⁺).

Compound 192 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.93 (s, 3H), 4.96 (s, 2H), 7.42-7.52 (m, 3H), 7.63-7.71 (m, 3H), 7.95-7.99 (m, 1H), 8.06-8.08 (dd, 2H), 8.20-8.23 (dd, 2H); MS: m/z 601.8 (MH⁺).

Compound 193 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.89 (s, 3H), 4.96 (s, 2H), 7.41-7.49 (m, 1H), 7.50-7.54 (m, 2H), 7.63-7.72 (m, 3H), 7.84-7.88 (t, 1H), 7.98-8.01 (m, 1H), 8.19-8.22 (m, 1H), 8.32-8.36 (m, 2H); MS: m/z 603.9 (MH⁺).

Compound 194 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluo ro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.93 (s, 3H), 4.96 (s, 2H), 7.43-7.54 (m, 3H), 7.65-7.74 (m, 3H), 7.96-7.99 (m, 1H), 8.06-8.08 (dd, 2H), 8.20-8.23 (dd, 2H); MS: m/z 558.0 (MH⁺).

Compound 195 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluo ro-3-trifluoromethyl-benzyl)-3-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.89 (s, 3H), 4.96 (s, 2H), 7.42-7.47 (t, 1H), 7.49-7.54 (m, 2H), 7.64-7.68 (m, 2H), 7.72-7.74 (m, 1H), 7.85-7.89 (m, 1H), 7.98-8.02 (m, 1H), 8.19-8.22 (m, 1H), 8.31-8.36 (m, 2H); MS: m/z 558.0 (MH⁺).

Compound 196 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.64 (s, 3H), 5.04 (s, 2H), 7.44-7.54 (m, 3H), 7.69-7.78 (m, 5H), 7.83-7.91 (m, 2H), 7.95-7.99 (m, 1H); MS: m/z 558.0 (MH⁺).

Compound 197 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.65 (s, 3H), 5.05 (s, 2H), 7.43-7.51 (m, 3H), 7.64-7.77 (m, 5H), 7.84-7.90 (m, 2H), 7.97-7.99 (m, 1H); MS: m/z 603.9 (MH⁺).

Compound 312 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-acetyl-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.67 (s, 3H), 4.95 (s, 2H), 7.44-7.51 (m, 3H), 7.67-7.72 (m, 3H), 7.80-8.07 (m, 3H), 8.19-8.21 (m, 2H); MS: m/z 585.9 (MH⁺).

Compound 317 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-N′,N′-dimethlysulfamide

¹H-NMR (DMSO-d₆): δ 2.94 (s, 6H), 4.87 (s, 2H), 7.41-7.52 (m, 3H), 7.64-7.73 (m, 3H), 7.96-7.99 (m, 1H); MS: m/z 511, 513.1 (MH⁺).

Compound 345 N-(3-Bromobenzo[b]thiophen-2-yl)-N-(butyl)-pyridin-3-yl-sulfonamide

¹H-NMR (DMSO-d₆): δ 0.83 (t, 3H), 1.49-1.29 (m, 4H), 3.70 (t, 2H), 7.60-7.50 (m, 2H), 7.74-7.68 (m, 1H), 7.81-7.75 (m, 1H), 8.06-7.98 (m, 1H), 8.29-8.23 (m, 1H), 9.00-8.92 (m, 2H); MS: m/z 425.0 (MH⁺).

Compound 350 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-C-methanesulfonyl-methanesulfonamide

MS: m/z 560, 562.0 (MH⁺), 582, 584.0 (MNa⁺).

Compound 576 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.98 (s, 2H), 7.38-7.55 (m, 3H), 7.61-7.74 (m, 3H), 7.90-8.01 (m, 2H), 8.14 (d, 1H), 8.48 (d, 1H), 8.55 (s, 1H); MS: m/z 612, 614.0 (MH⁺).

Compound 578 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.98 (s, 2H), 7.35-7.58 (m, 3H), 7.63-7.78 (m, 3H), 7.90-8.03 (m, 2H), 8.14 (d, 1H), 8.49 (d, 1H), 8.55 (s, 1H); MS: m/z 567.6 (MH⁺).

Compound 594 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.014-0.065 (m, 3H), 0.343-0.388 (m, 2H), 0.713-0.813 (m, 1H), 1.35-1.40 (m, 2H), 3.72-3.76 (t, 2H), 7.51-7.57 (m, 2H), 7.73-7.79 (m, 1H), 7.96-8.03 (m, 1H), 8.06-8.08 (d, 2H), 8.30-8.32 (d, 2H); MS: m/z 505.6 (MH⁺).

Compound 595 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.57-2.67 (m, 2H), 3.96-4.02 (t, 2H), 7.53-7.57 (m, 2H), 7.74-7.77 (m, 1H), 8.00-8.04 (m, 1H), 8.07-8.09 (d, 2H), 8.29-8.31 (m, 2H); MS: m/z 533.5 (MH⁺).

Compound 635 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.008-0.034 (m, 3H), 0.346-0.392 (m, 2H), 0.719-0.794 (m, 1H), 1.35-1.40 (m, 2H), 3.72-3.75 (t, 2H), 7.52-7.57 (m, 2H), 7.77-7.82 (m, 1H), 7.98-8.01 (m, 1H), 8.02-8.09 (m, 2H), 8.29-8.32 (m, 2H); MS: m/z 459.7 (MH⁺).

Compound 636 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.55-2.67 (m, 2H), 3.97-4.01 (t, 2H), 7.52-7.58 (m, 2H), 7.76-7.82 (m, 1H), 8.00-8.05 (m, 1H), 8.07-8.09 (m, 2H), 8.29-8.31 (d, 2H); MS: m/z 487.6 (MH⁺).

Compound 702 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2,2,2-trifluoro-ethanesulfonamide

¹H-NMR (CDCl₃): δ 4.07 (q, 2H), 4.96 (s, 2H), 7.12 (t, 1H), 7.42-7.55 (m, 4H), 7.65-7.76 (m, 1H), 7.76-7.86 (m, 1H); MS: m/z 573.9 (MNa⁺).

Compound 703 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2,2,2-trifluoro-ethanesulfonamide

MS: m/z 528.0 (MNa⁺).

Compound 706 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.013-0.050 (m, 2H), 0.314-0.376 (m, 2H), 0.695-0.794 (m, 1H), 1.33-1.38 (m, 2H), 3.70-3.74 (m, 2H), 7.50-7.56 (m, 2H), 7.73-7.78 (m, 1H), 7.96-7.98 (m, 1H), 8.00-8.01 (d, 2H), 8.18-8.20 (d, 2H), 13.69 (s, 1H); MS: m/z 538.0 (MH⁺).

Compound 707 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-2-fluoro-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.58-1.75 (m, 4H), 2.18-2.28 (m, 2H), 3.85-3.87 (m, 2H), 7.51-7.55 (m, 2H), 7.72-7.76 (m, 1H), 7.85-7.90 (m, 2H), 7.94-8.04 (m, 2H), 13.88 (s, 1H); MS: m/z 555.9 (MH⁺).

Compound 708 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.55-2.66 (m, 2H), 3.98-4.01 (t, 2H), 7.53-7.57 (m, 2H), 7.74-7.78 (m, 1H), 8.00-8.04 (m, 3H), 8.18-8.20 (d, 2H), 13.70 (s, 1H); MS: m/z 566.0 (MH⁺).

Compound 709 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-2-fluoro-4-curb oxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.000-0.005 (m, 2H), 0.292-0.373 (m, 2H), 0.670-0.769 (m, 1H), 1.36-1.41 (m, 2H), 3.84-3.87 (t, 2H), 7.47-7.52 (m, 2H), 7.68-7.74 (m, 1H), 7.81-7.86 (m, 2H), 7.91-7.99 (m, 2H), 13.84 (s, 1H); MS: m/z 500.0 (MH⁺).

Compound 710 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-2-fluoro-4-curb oxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.58-2.68 (m, 2H), 4.12-4.16 (t, 2H), 7.51-7.57 (m, 2H), 7.71-7.77 (m, 1H), 7.83-7.89 (m, 2H), 7.96-8.06 (m, 2H), 13.89 (s, 1H); MS: m/z 528.0 (MH⁺).

Compound 711 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-fluoro-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 5.08 (s, 2H), 7.45-7.52 (m, 3H), 7.65-7.69 (m, 3H), 7.89-8.01 (m, 4H), 13.92 (s, 1H); MS: m/z 608.0 (MH⁺).

Compound 712 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.52-1.63 (m, 4H), 2.21-2.28 (m, 2H), 3.70 (m, 2H), 7.51-7.58 (m, 2H), 7.77-7.80 (m, 1H), 7.98-8.02 (m, 3H), 8.19-8.21 (m, 2H), 13.70 (s, 1H); MS: m/z 594.0 (MH⁺).

Compound 785 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.93 (s, 3H), 4.68-4.96 (s, 2H), 7.23-7.35 (m, 2H), 7.36-7.42 (m, 4H), 7.65-7.68 (m, 1H), 7.80-7.84 (m, 1H), 8.10-8.12 (d, 2H), 8.31-8.33 (d, 2H); MS: m/z 546.0 (MH⁺).

Example 12

Compound 198 N-(3-Cyano-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-ethanesulfonamide

A mixture of compound 183 (97 mg, 0.195 mmol) and CuCN (44 mg, 0.496 mmol) in DMF (3 mL) was heated at reflux for 6 h. The mixture was cooled, an additional portion of CuCN (55 mg, 0.614 mmol) was added, and the reaction heated overnight. The mixture was cooled, and the inorganics were removed by filtration. The resultant solution was partitioned between ethyl acetate and water. The organic layer was separated, washed with water (3×), brine, dried over sodium sulfate, filtered, and the solvent was evaporated in vacuo. The crude residue was purified by HPLC (C₁₈) eluting with a acetonitrile-water (0.1% TFA) (10-40%) gradient, to afford compound 198 as an oil (40 mg, 46%). ¹H-NMR (DMSO-d₆): δ 1.39 (t, 3H), 3.62 (q, 2H), 5.09 (s, 2H), 7.49 (t, 1H), 7.54-7.61 (m, 2H), 7.68-7.72 (m, 1H), 7.78-7.83 (m, 2H), 8.09-8.13 (m, 1H); MS: m/z 443.1 (MH⁺).

Example 13

Compound 199 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-pyrimidin-5-yl-benzo[b]thiophen-2-yl)-ethanesulfonamide

A solution of compound 183 (140 mg, 0.28 mmol) and 5-pyrimidineboronic acid (42 mg, 0.34 mmol) in dioxane (2 mL) was treated with 2 M sodium carbonate (352 mL, 0.705 mmol) and palladium catalyst (Johnson Matthey Pd(118), 10 mg, 0.015 mmol). Dioxane was added, the tube was purged with argon, sealed and heated to 80° C. for 2 h. The solvent was evaporated in vacuo, and the residue partitioned between dichloromethane and water. The organic layer was separated, dried over sodium sulfate, filtered, and the solvent evaporated in vacuo. The residue was purified by HPLC (C₁₈) eluting with an acetonitrile-water (0.1% TFA) (30-90%) to afford compound 199 as a brown oil (19 mg, 14%). ¹H-NMR (DMSO-d₆): δ 1.35 (t, 3H), 3.58 (q, 2H), 4.77 (s, 2H), 7.24-7.42 (m, 5H), 7.49-7.56 (m, 1H), 8.09 (d, 1H), 8.50 (s, 2H), 9.15 (s, 1H); MS: m/z 496.2 (MH⁺).

Following the procedure described above for example 13 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 200 N-[3-(2-Fluoro-phenyl)-benzo[b]thiophen-2-yl]-N-(4-fluoro-3-trifluoromethyl-benzyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.26 (t, 3H), 3.44 (q, 2H), 4.61 (d, 1H), 4.86 (d, 1H), 7.09-7.19 (m, 2H), 7.23-7.30 (m, 2H), 7.33-7.51 (m, 6H), 8.00 (d, 1H); MS: m/z 512.3 (MH⁺).

Compound 201 N-[3-(4-Fluoro-phenyl)-benzo[b]thiophen-2-yl]-N-(4-fluoro-3-trifluoromethyl-benzyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.30 (t, 3H), 3.47 (q, 2H), 4.71 (s, 2H), 7.15-7.40 (m, 9H), 7.44-7.50 (m, 1H), 8.00 (d, 1H); MS: m/z 512.2 (MH⁺).

Compound 202 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-thiophen-3-yl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.27 (t, 3H), 3.39 (q, 2H), 4.76 (s, 2H), 7.06 (d, 1H), 7.28 (t, 1H), 7.36-7.52 (m, 5H), 7.55-7.58 (m, 1H), 7.62-7.65 (m, 1H), 7.97 (d, 1H); MS: m/z 500.1 (MH⁺).

Example 14

Compound 203 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-formyl-benzo[b]thiophen-2-yl)-4-carbomethoxybenzenesulfonamide

A solution of acetylchloride (16 μL, 0.224 mmol) in dichloromethane (3 mL), at 0° C., was treated with tin(IV)chloride (26 μL, 0.224 mmol) and the resultant solution was stirred at 0° C. for 15 min. Compound 35 (75 mg, 0.204 mmol) was added to the solution and the mixture stirred at ambient temperature overnight. The reaction mixture was washed with 2 N HCl, dried over sodium sulfate, filtered, and the solvent evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂) eluting with an ethyl acetate-heptane (10-80%) gradient. The product was further purified by HPLC (C₁₈) eluting with an acetonitrile-water (0.1% TFA) (40-90%) gradient to afford compound 203 as a colorless solid (25 mg, 30%). ¹H-NMR (DMSO-d₆): δ 1.31 (t, 3H), 2.30 (s, 3H), 3.47 (q, 2H), 4.98 (s, 2H), 7.17 (m, 1H), 7.35 (m, 4H), 7.94-8.03 (m, 2H); MS: m/z 410.1 (MH⁺).

Following the procedure described above for example 14 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 204 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.37 (s, 3H), 4.86 (br s, 2H), 7.16-7.24 (m, 1H), 7.33-7.49 (m, 4H), 7.65-7.73 (m, 2H), 7.82-7.86 (m, 3H), 7.90-7.96 (m, 1H), 7.99-8.04 (m, 1H); MS: m/z 458.3 (MH⁺).

Compound 833 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(3-fluoro-propyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.08-2.21 (m, 2H), 2.79 (s, 3H), 3.81 (s, 2H), 4.48 (t, 1H), 4.61 (t, 1H), 7.41-7.78 (m, 8H), 8.25 (m, 1H).

Example 15

Compound 205-A was prepared from compound 1-C and 4-ethanesulfonyl chloride, following the procedure used to prepare compound 1-D.

N-(3-Acetyl-benzo[b]thiophen-2-yl)-ethanesulfonamide (205-B)

Tin(IV)chloride (173 μL, 1.48 mmol) was added to a solution of acetyl chloride (124 μL, 1.75 mmol) in dichloromethane (10 mL), at 0° C., and the solution was stirred for 5 min. To the reaction mixture was added a solution of compound 205-A (325 mg, 1.35 mmol) in dichloromethane (2 mL) at 0° C. The resultant solution was allowed to warm to ambient temperature and stirred overnight. The solution was treated with water (10 mL), the organic layer separated, dried over sodium sulfate, filtered, and the solvent evaporated in vacuo to afford compound 205-B as a colorless solid (355 mg, 93%). ¹H-NMR (DMSO-d₆): δ 1.25 (t, 3H), 2.71 (s, 3H), 3.39 (q, 2H), 7.34-7.48 (m, 2H), 7.94 (d, 1H), 8.10 (d, 1H); MS: m/z 284.1 (MH⁺).

Compound 205 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-ethanesulfonamide

Sodium hydride (60% in oil, 46 mg, 1.15 mmol) was added to a solution of compound 205-B (310 mg, 1.09 mmol) in DMF (4 mL), at 0° C. The resultant mixture was stirred at 0° C. for 15 min, to which was added 4-fluoro-3-trifluoromethylbenzyl bromide (253 μL, 1.33 mmol) and the resultant mixture was stirred at ambient temperature for 2 h. 15-Crown-5 (220 μL, 1.33 mmol) and an additional equivalent of 4-fluoro-3-trifluoromethylbenzyl bromide was added to the reaction mixture. The resultant solution was stirred at ambient temperature overnight, water added, and the product extracted into ethyl acetate. The organic phase was washed with water (3×), brine, dried over sodium sulfate, filtered, and the solvent evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂), eluting with an ethyl acetate-heptane gradient to afford compound 205 as an off-white solid (285 mg, 57%). ¹H-NMR (DMSO-d₆): δ 1.32 (t, 3H), 2.29 (s, 3H), 3.49 (q, 2H), 5.08 (s, 2H), 7.41-7.52 9m, 3H), 7.70-7.77 (m, 2H), 7.93-8.03 (m, 2H); MS: m/z 460.2 (MH⁺).

Following the procedure described above for example 15 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 313 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.36 (s, 3H), 3.92 (s, 3H), 4.99 (s, 2H), 7.41-7.48 (m, 3H), 7.67-7.73 (m, 2H), 7.91-8.00 (m, 4H), 8.21 (d, 2H); MS: m/z 566.2 (MH⁺).

Compound 314 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.38 (s, 3H), 4.95 (s, 2H), 7.41-7.48 (m, 3H), 7.68-7.75 (m, 4H), 7.80-7.87 (m, 3H), 7.91-7.96 (m, 1H), 8.00-8.04 (m, 1H); MS: m/z 508.2 (MH⁺).

Compound 837 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-methoxy-benzyl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.46 (t, 3H), 2.36 (s, 3H), 3.19 (q, 2H), 3.81 (s, 3H), 4.91 (s, 2H), 6.82-6.86 (m, 1H), 6.97 (dd, 1H), 7.03 (dd, 1H), 7.40-7.44 (m, 2H), 7.72-7.75 (m, 1H), 8.07-8.11 (m, 1H); MS: m/z 444.1 (MNa⁺).

Example 16

Compound 206 N-(3,4-Difluoro-benzyl)-N-(3-formyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

A solution of titanium(IV) chloride (1.0 M in dichloromethane, 0.94 mL, 0.94 mmol) was added to a solution of compound 1 (270 mg, 0.65 mmol) in dichloromethane (6 mL), at −5° C. The resultant solution was stirred at −5° C. for 15 min to which was added α,α-dichloromethylmethyl ether (75 mL, 0.845 mmol) and the reaction mixture was stirred at ambient temperature overnight. The solution was treated with 2N HCl (10 mL), the organic layer separated, dried over sodium sulfate, filtered, and the solvent evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂), eluting with an ethyl acetate-heptane gradient (10-40%) to afford compound 206 as a colorless solid (180 mg, 62%). ¹H-NMR (DMSO-d₆): δ 4.94 (s, 2H), 7.15-7.25 (m, 1H), 7.33-7.55 (m, 4H), 7.68-7.72 (m, 2H), 7.83-7.87 (m, 3H), 7.98-8.01 (m, 1H), 8.43-8.46 (m, 1H), 9.87 (s, 1H); MS: m/z 444.1 (MH⁺).

Following the procedure described above for example 16 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 207 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-formyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 5.06 (br s, 2H), 7.43-7.55 (m, 3H), 7.68-7.79 (m, 4H), 7.83-7.89 (m, 3H), 7.98-8.03 (m, 1H), 8.42-8.47 (m, 1H), 9.84 (s, 1H); MS: m/z 494.1 (MH⁺).

Compound 208 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-formyl-benzo[b]thiophen-2-yl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 3.45 (s, 3H), 5.11 (s, 2H), 7.44-7.55 (m, 3H), 7.73-7.79 (m, 2H), 8.04-8.09 (m, 1H), 8.42-8.46 (m, 1H), 9.91 (s, 1H); MS: m/z 432.0 (MH⁺).

Compound 209 N-(3,4-Difluoro-benzyl)-N-(3-formyl-benzo[b]thiophen-2-yl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 3.43 (s, 3H), 5.00 (s, 2H), 7.19-7.26 (m, 1H), 7.33-7.55 (m, 4H), 8.03-8.09 (m, 1H), 8.42-8.47 (m, 1H), 9.91 (s, 1H); MS: m/z 382.2 (MH⁺).

Compound 210 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-formyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.36 (t, 3H), 3.61 (q, 2H), 5.15 (s, 2H), 7.45-7.55 (m, 3H), 7.71-7.78 (m, 2H), 8.03-8.10 (m, 1H), 8.40-8.47 (m, 1H), 9.83 (s, 1H); MS: m/z 446.1 (MH⁺).

Compound 211 N-(3-Formyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.93 (s, 3H), 5.08 (s, 2H), 7.44-7.55 (m, 3H), 7.70-7.81 (m, 2H), 7.99-8.05 (m, 3H), 8.22 (d, 2H), 8.42-8.46 (m, 1H), 9.85 (s, 1H); MS: m/z 552.2 (MH⁺).

Compound 212 N-(3,4-Difluoro-benzyl)-N-(3-formyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.36 (t, 3H), 3.61 (q, 2H), 5.04 (s, 2H), 7.17-7.24 (m, 1H), 7.34-7.46 (m, 2H), 7.48-7.54 (m, 2H), 8.03-8.08 (m, 1H), 8.40-8.46 (m, 1H), 9.83 (s, 1H); MS: m/z 396.1 (MH⁺).

Compound 419 N-(Butyl)-N-(3-formyl-benzo[b]thiophene-2-yl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 432.1 (MH⁺).

Example 17

Compound 213 N-(3,4-Difluoro-benzyl)-N-(3-hydroxymethyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

Sodium borohydride (25 mg, 0.66 mmol) was added to a solution of compound 206 (50 mg, 0.112 mmol) in ethanol (2 mL), and the mixture was stirred at rt for 3 h. The solvent was evaporated, the residue partitioned between dichloromethane and water, the organic layer separated, dried over sodium sulfate, filtered, and the solvent evaporated in vacuo. The residue was purified by flash column chromatography (SiO₂), eluting with an ethyl acetate-heptane (10-40%) gradient to afford compound 213 as a colorless solid (42 mg, 84%). ¹H-NMR (DMSO-d₆): δ 4.26 (d, 2H, collapses to singlet with D₂O), 4.80 (s, 2H), 5.01 (t, 1H, exchanges with D₂O), 7.10-7.14 (m, 1H), 7.25-7.40 (m, 4H), 7.67 (t, 2H), 7.78-7.86 (m, 4H), 7.90-7.96 (m, 1H); MS: m/z 428.0 (M-OH)⁺, 468.0 (MNa⁺).

Following the procedure described above for example 17 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 214 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-hydroxymethyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.29 (d, 2H), 4.90 (s, 2H), 5.02 (t, 1H), 7.35-7.45 (m, 3H), 7.61-7.71 (m, 4H), 7.78-7.87 (m, 4H), 7.90-7.95 (m, 1H); MS: m/z 478.0 [(M-OH)⁺], 518 (MNa⁺).

Compound 215 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-hydroxymethyl-benzo[b]thiophen-2-yl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 3.32 (s, 3H), 4.55 (d, 2H), 4.92 (s, 2H), 5.10 (t, 1H), 7.36-7.50 (m, 3H), 7.65-7.72 (m, 2H), 7.84-7.90 (m, 1H), 7.93-7.98 (m, 1H); MS: m/z 416.1 (M-OH)⁺, 456.1 (MNa⁺).

Compound 216 N-(3,4-Difluoro-benzyl)-N-(3-hydroxymethyl-benzo[b]thiophen-2-yl)-methanesulfonamide

¹H-NMR (CDCl₃): δ 2.49 (t, 1H), 3.11 (s, 3H), 4.44 (d, 2H), 4.77 (br s, 2H), 7.02-7.20 (m, 3H), 7.40-7.46 (m, 2H), 7.74-7.80 (m, 1H), 7.88-7.94 (m, 1H); MS: m/z 366.1 (M-OH)⁺, 406.0 (MNa⁺).

Compound 217 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-hydroxymethyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.33 (t, 3H), 3.47 (q, 2H), 4.53 (d, 2H), 4.93 (s, 2H), 5.09 (t, 1H), 7.36-7.50 (m, 3H), 7.62-7.71 (m, 2H), 7.83-7.90 (m, 1H), 7.92-7.98 (m, 1H); MS: m/z 430.2 (M-OH)⁺, 470.1 (MNa⁺).

Compound 218 N-(3-Hydroxymethyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.98 (br s, 1H), 4.29 (s, 2H), 4.93 (s, 2H), 7.34-7.48 (m, 3H), 7.59-7.68 (m, 2H), 7.82-7.87 (m, 1H), 7.91-8.00 (m, 1H) superimposed on 7.98 (d, 2H), 8.18 (d, 2H), 13.63 (br s, 1H); MS: m/z 522.2 (M-OH)⁺, 562.2 (MNa⁺).

Compound 219 N-(3,4-Difluoro-benzyl)-N-(3-hydroxymethyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.33 (t, 3H), 3.46 (q, 2H), 4.54 (d, 2H), 4.84 (s, 2H), 5.09 (t, 1H), 7.10-7.17 (m, 1H), 7.29-7.42 (m, 4H), 7.83-7.89 (m, 1H), 7.93-7.98 (m, 1H); MS: m/z 380.1 (M-OH)⁺, 420.1 (MNa⁺).

Compound 220 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-[3-(1-hydroxy-ethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.08 (br s, 3H), 1.50 (t, 3H), 3.27 (q, 2H), 4.42 (d, 1H), 4.94 (q, 1H), 5.29 (d, 1H), 7.13 (t, 1H), 7.35-7.40 (m, 2H), 7.49-7.54 (m, 2H), 7.58 (d, 1H), 7.74-7.77 (m, 1H), 8.12 (br d, 1H); MS: m/z 444.1 (M-OH)⁺, 484.2 (MNa⁺). Compound 220 (143 mg) was separated by chiral HPLC (Chiralpak IA) eluting with 100% MeOH to afford 54.4 mg of compound 534 and 48.0 mg of compound 535 as clear oils.

Compound 534 N-(4-Fluoro-3-trifluoromethyl-benzyl)-(S)—N-[3-(1-hydroxy-ethyl)-(benzo[b]thiophen-2-yl)-ethyl-sulfon amide

¹H-NMR (DMSO-d₆): δ 1.32-1.36 (t, 3H), 3.16-3.17 (d, 1H), 3.44-3.50 (m, 2H), 4.05-4.09 (m, 1H), 4.85-4.98 (m, 4H), 5.11 (s, 1H), 7.32-7.39 (m, 2H), 7.43-7.48 (m, 1H), 7.64-7.70 (m, 2H), 7.85-7.87 (m, 1H), 8.14-8.16 (m, 1H); MS: m/z 444.0 (M-OH)⁺.

Compound 535 N-(4-Fluoro-3-trifluoromethyl-benzyl)-(R)—N-[3-(1-hydroxy-ethyl)-(benzo[b]thiophen-2-yl)-ethyl-sulfon amide

¹H-NMR (DMSO-d₆): δ 1.32-1.36 (t, 3H), 3.16-3.17 (d, 1H), 3.45-3.50 (m, 2H), 4.08 (m, 1H), 4.85-5.02 (m, 4H), 5.11 (s, 1H), 7.33-7.39 (m, 2H), 7.43-7.48 (m, 1H), 7.64-7.71 (m, 2H), 7.85-7.87 (m, 1H), 8.14-8.17 (m, 1H); MS: m/z 444.0 (M-OH)⁺.

Compound 221 N-(3,4-Difluoro-benzyl)-N-[3-(1-hydroxy-ethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

¹H-NMR (DMSO-d₆) δ: 1.02-1.55 (br s, 3H) superimposed on 1.34 (t, 3H), 3.46 (q, 2H), 4.78 (br s, 2H), 4.94-5.04 (m, 1H), 5.12 (s, 1H), 7.11-7.19 (m, 1H), 7.30-7.42 (m, 4H), 7.84-7.89 (m, 1H), 8.13-8.20 (m, 1H); MS: m/z 394.2 (M-OH)⁺, 434.1 (MNa⁺).

Compound 335 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-[3-(1-hydroxy-ethyl)-benzo[b]thiophen-2-yl]-4-carboxybenzenesulfonamide

¹H-NMR (CDCl₃): δ 1.15 (d, 3H), 5.03-5.47 (m, 3H), 7.18 (t, 1H), 7.32-7.70 (m, 5H), 7.87-8.00 (m, 2H), 8.12-8.20 (m, 1H), 8.27 (d, 2H); MS: m/z 536 (M-OH)⁺, 576 (MNa⁺).

Compound 821 N-(3-Fluoropropyl)-N-(3-hydroxymethyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.95 (dtt, 2H), 2.96 (t, 1H), 3.51-3.91 (br, 2H), 4.52 (dt, 2H), 4.89 (br d, 2H), 7.41 (dt, 1H), 7.48 (dt, 1H), 7.55 (t, 2H), 7.68-7.72 (m, 2H), 7.75-7.77 (m, 2H), 8.02-8.04 (m, 1H); MS: m/z 402.0 (MNa⁺).

Compound 834 2,5-Dibromo-N-(3,4-difluoro-benzyl)-N-(3-hydroxymethyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

MS: m/z 624.2, 626.2, 628.2 (MNa⁺).

Example 18

Compound 222 N-(3,4-Difluoro-benzyl)-N-[3-(1-hydroxy-ethyl)-benzo[b]thiophen-2-yl]-benzenesulfonamide

A solution of methylmagnesium bromide in THF/toluene (1.4 M, 0.31 mL, 0.41 mmol) was added to a solution of compound 206 (120 mg, 0.270 mmol) in THF (3 mL) at 0° C. The resultant solution was stirred at ambient temperature for 3 h, then treated with a saturated aqueous solution of ammonium chloride. The product was extracted into ethyl acetate, washed with brine, dried over sodium sulfate, filtered, and the solvent evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂), eluting with an ethyl acetate-heptane (10-40%) gradient to afford compound 222 as a colorless solid (103 mg, 83%). ¹H-NMR (DMSO-d₆): δ 0.65-1.50 (br m, 3H), 4.53-4.73 (br s, 1 h), 4.75-4.97 (br s, 2H), 5.08 (d, 1H, exchanges with D₂O), 7.01-7.12 (m, 1H), 7.19-7.40 (m, 4H), 7.68 (t, 2H), 7.78-7.82 (d of d, 2H), 7.90 (d, 2H), 8.12-8.16 (m, 1 h); MS: m/z 442 (M-OH)⁺, 482.1 (MNa⁺).

Following the procedure described above for example 18 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared.

Compound 223 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-[3-(1-hydroxy-ethyl)-benzo[b]thiophen-2-yl]-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.10-1.28 (m, 3H), 2.64 (br s, 1H, exchanges with D₂O), 4.06-4.21 (m, 1H), 5.05-5.34 (m, 2H), 7.09 (t, 1H), 7.31-7.39 (m, 2H), 7.43-7.50 (m, 1H), 7.52-7.85 (m, 7H), 8.11-8.19 (m, 1H); MS: m/z 492.0 [(M-OH)⁺], 532.0 (MNa⁺).

Compound 224 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-[3-(1-hydroxy-ethyl)-benzo[b]thiophen-2-yl]-methanesulfonamide

¹H-NMR (CDCl₃): δ 1.06-1.29 (br m, 3H), 2.53 (br s, 1H), 3.10 (s, 3H), 4.38 (br d, 1H), 4.98-5.30 (br m, 2H), 7.14 (t, 1H), 7.34-7.42 (m, 2H), 7.49-7.56 (m, 1H), 7.56-7.62 (m, 1H), 7.73-7.79 (m, 1H), 8.09-8.16 (m, 1H); MS: m/z 430 [(M-OH)⁺], 470.2 (MNa⁺).

Compound 225 N-(3,4-Difluoro-benzyl)-N-[3-(1-hydroxy-ethyl)-benzo[b]thiophen-2-yl]-methanesulfonamide

¹H-NMR (CDCl₃): δ 1.06-1.63 (br m, 3H), 2.52 (br s, 1H), 4.32 (br d, 1H), 3.08 (s, 3H), 4.95-5.24 (br m, 2H), 7.01-7.24 (m, 3H), 7.34-7.41 (m, 2H), 7.73-7.79 (m, 1H), 8.09-8.17 (m, 1H); MS: m/z 380.1 [(M-OH)⁺], 420.1 (MNa⁺).

Compound 316 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-[3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl]-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.35 (s, 3H), 1.62 (s, 3H), 4.53-4.61 (m, 1H), 5.04-5.61 (m, 2H), 7.30-7.50 (m, 5H), 7.65-7.90 (m, 6H), 8.40 (s, 1H); MS: m/z 506.2 (M-OH)⁺.

Compound 821 N-(3-Fluoropropyl)-N-[3-(1-hydroxyethyl)-benzo[b]thiophen-2-yl]-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.60-2.10 (m, 5H), 2.71 (br s, 1H), 3.12-3.20 (m, 1H), 4.02-4.15 (m, 1H), 4.34-4.56 (m, 2H), 5.38-5.46 (m, 1H), 7.26-7.36 m, 2H), 7.43-7.47 (m, 2H), 7.57-7.61 (m, 2H), 7.65-7.72 (m, 2H), 8.16-8.21 (m, 1H); MS: m/z 416.0 (MNa⁺).

Compound 827 N-(4-Fluoro-3-methoxybenzyl)-N-[3-(1-hydroxyethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.10 (br s, 3H), 1.52 (t, 3H), 2.65 (br s, 1H), 3.27 (br q, 2H), 3.86 (br s, 3H), 4.35-4.39 (br m, 1H), 4.95-5.00 (m, 1H), 5.21-5.25 (m, 1H), 6.73-6.77 (m, 1H), 6.95 (dd, 1H), 7.02 (dd, 1H), 7.35-7.42 (m, 2H), 7.75-7.78 (m, 1H), 8.12-8.14 (m, 1H); MS: m/z 446.4 (MNa⁺).

Compound 835 N-(2-Fluoropyridin-4-ylmethyl)-N-[3-(1-hydroxyethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

MS: m/z 395.2 (MH⁺).

Example 19

Compound 226 N-(3,4-Difluoro-benzyl)-N-[3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

A solution of methylmagnesium bromide in THF/toluene (1.4 M, 0.21 mL, 0.29 mmol) was added to a solution of compound 203 (0.10 g, 0.24 mmol) in THF (2 mL), at 0° C. and the resultant solution was stirred at ambient temperature for 2 h. An additional portion of methylmagnesium bromide in THF/toluene (1.4 M, 0.21 mL, 0.29 mmol) was added, and the resultant solution stirred at rt for an additional 18 h, and the solution was quenched with a saturated aqueous solution of ammonium chloride. The product was extracted into ethyl acetate, washed with brine and dried over sodium sulfate, filtered, and the solvent evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂), eluting with an ethyl acetate-heptane (10-30%) gradient to afford compound 226 as a colorless solid (66 mg, 65%). ¹H-NMR (DMSO-d₆): δ 1.30 (t, 3H), 1.41 (s, 3H), 1.60 (s, 3H), 3.31-3.45 (m, 2H), 4.74 (d, 1H), 4.86 (d, 1H), 5.14 (s, 1H), 7.11-7.17 (m, 1H), 7.31-7.45 (m, 4H) 7.79-7.85 (m, 1H), 8.31-8.36 (m, 1H); MS: m/z 408.1 [(M-OH)⁺], 448.2 (MNa⁺).

Following the procedure described above for example 19 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared.

Compound 227 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-[3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.41 (t, 3H), 1.49 (s, 3H), 1.75 (s, 3H), 3.16-3.36 (m, 2H), 3.65 (s, 1H), 4.87 (d, 1H), 4.98 (d, 1H), 7.12 (t, 1H), 7.34-7.40 (m, 2H), 7.55-7.72 (m, 3H), 7.87-7.92 (m, 1H); MS: m/z 458.1 [(M-OH)⁺], 498.1 (MNa⁺).

Compound 776 N-(2-Fluoro-3-methoxy-benzyl)-N-[3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.45 (t, 3H), 1.61 (s, 3H), 1.76 (s, 3H), 3.25-3.40 (m, 2H), 3.54 (s, 1H), 3.82-3.89 (m, 3H), 4.90-5.14 (m, 2H), 6.82-6.99 (m, H), 7.28-7.38 (m, 2H), 7.60-7.68 (m, 1H), 7.88-7.97 (m, 1H); MS: m/z 420.1 (M-OH)⁺.

Compound 802 N-[3-(1-Hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl]-N-(2,4,5-trifluoro-3-methoxy-benzyl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.45 (t, 3H), 1.59 (s, 3H), 1.79 (s, 3H), 3.31 (qd, 2H), 3.73 (s, 1H), 3.97 (s, 3H), 4.96 (s, 2H), 6.95 (ddd, 1H), 7.31-7.43 (m, 2H), 7.63-7.73 (m, 1H), 7.85-7.94 (m, 1H); MS: m/z 456.03 (M-OH)⁺.

Compound 830 N-(3-Fluoropropyl)-N-[3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl]-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.79 (s, 3H), 1.92 (s, 3H), 1.94-2.21 (m, 2H), 3.44-3.52 (m, 1H), 3.59 (s, 1H), 4.14-4.22 (m, 1H), 4.45-4.75 (m, 2H), 7.33-7.42 (m, 2H), 7.54 (t, 2H), 7.61-7.63 (m, 1H), 7.69 (t, 1H), 7.79-7.81 (m, 2H), 8.03 (d, 1H); MS: m/z 430.0 (MNa⁺).

Compound 836 N-(2-Fluoro-pyridin-4-ylmethyl)-N-[3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.43 (t, 3H), 1.57 (s, 3H), 1.80 (s, 3H), 3.22-3.38 (m, 2H), 3.77 (s, 1H), 4.90-4.95 (m, 2H), 7.05 (s, 1H), 7.26-7.28 (m, 1H), 7.35-7.40 (m, 2H), 7.67-7.71 (m, 1H), 7.87-7.90 (m, 1H), 8.16 (d, 1H). MS: m/z 409.4 (MH⁺).

Compound 838 N-(4-Fluoro-3-methoxybenzyl)-N-[3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.41 (t, 3H), 1.52 (s, 3H), 1.72 (s, 3H), 3.16-3.32 (m, 2H), 3.48 (s, 1H), 3.82 (s, 3H), 4.78 (d, 1H), 4.92 (d, 1H), 6.77-6.81 (m, 1H), 6.93 (dd, 1H), 7.09 (dd, 1H), 7.33-7.38 (m, 2H), 7.68-7.71 (m, 1H), 7.92-7.96 (m, 1H); MS: m/z 897.2 (M₂Na⁺).

Example 20

Compound 228 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-methanesulfonamide

Pyridinium chlorochromate (0.205 g, 0.955 mmol) was added to a solution of compound 224 (0.285 g, 0.637 mmol) in dichloromethane (10 mL) and stirred at rt for 18 h. The mixture was washed with water, absorbed onto silica gel, and the product isolated by flash column chromatography (SiO₂), eluting with an ethyl acetate-heptane (10-70%) gradient to afford compound 228 as a colorless solid (0.228 g, 80%). ¹H-NMR (DMSO-d₆): δ 2.31 (s, 3H), 3.34 (s, 3H), 5.03 (s, 2H), 7.43-7.52 (m, 3H), 7.70-7.78 (m, 2H), 7.97-8.03 (m, 2H); MS: m/z 446.1 (MH⁺).

Following the procedure described above for example 20 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared.

Compound 229 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 2.31 (s, 3H), 3.32 (s, 3H), 4.94 (s, 2H), 7.18-7.24 (m, 1H), 7.36-7.50 (m, 4H), 7.87-8.04 (m, 2H); MS: m/z 396.1 (MH⁺).

Example 21

Compound 230 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5-carboethoxy-pentyl)benzenesulfonamide

To a stock solution of Ph₃P in THF (1.0 mL, 0.375 M, 0.375 mmol) was added THF (2 mL) and a solution of DEAD (0.17 mL, 40% in toluene, 0.38 mmol). After stirring for a few minutes, compound 1-D (0.072 g, 0.25 mmol) was added followed by 6-hydroxy-hexanoic acid ethyl ester (0.049 mL, 0.30 mmol), and the reaction mixture was stirred overnight. The reaction mixture was evaporated in vacuo and the crude residue was dissolved in 1:1 dichloroethane/acetic acid (2 mL), to which was added NBS (0.053 g, 0.30 mmol). After stirring for 6 h the reaction mixture was evaporated in vacuo and purified by reverse-phase chromatography (25-95% acetonitrile/water+0.1% TFA) to afford compound 230 as a waxy tan solid (0.090 g, 0.18 mmol). ¹H-NMR (DMSO-d₆): δ 1.14 (t, 3H), 1.28-1.52 (m, 6H), 2.21 (t, 2H), 3.59 (br t, 2H), 4.01 (q, 2H), 7.50-7.59 (m, 2H), 7.66 (t, 2H), 7.75-7.82 (m, 2H), 7.85 (d, 2H), 7.96-8.03 (m, 1H); MS: m/z 510.1 (MH⁺).

Following the procedure described above for example 21 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared.

Compound 231 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.81 (t, 3H), 1.28-1.45 (m, 4H), 3.60 (br t, 2H), 7.49-7.58 (m, 2H), 7.67 (t, 2H), 7.75-7.82 (m, 2H), 7.85 (dd, 2H), 7.97-8.02 (m, 1H); MS: m/z 424.1 (MH⁺).

Compound 232 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclohexylmethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.87-1.00 (m, 2H), 1.01-1.16 (m, 3H), 1.23-1.35 (m, 1H), 1.52-1.67 (m, 3H), 1.77 (br s, 2H), 3.44 (br s, 2H), 7.49-7.58 (m, 2H), 7.65 (t, 2H), 7.73-7.85 (m, 4H), 7.96-8.02 (m, 1H); MS: m/z 464.0 (MH⁺).

Compound 233 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(phenethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.81 (t, 2H), 3.86 (t, 2H), 7.13-7.29 (m, 5H), 7.50-7.58 (m, 2H), 7.64 (t, 2H), 7.73-7.86 (m, 4H), 7.79-8.04 (m, 1H); MS: m/z 472.1 (MH⁺).

Compound 234 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-tert-butoxy-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.98 (s, 9H), 3.41 (t, 2H), 3.79 (t, 2H), 7.48-7.56 (m, 2H), 7.64 (t, 2H), 7.71-7.79 (m, 2H), 7.83-7.89 (m, 2H), 7.97-8.02 (m, 1H); MS: m/z 490.0 (MNa⁺).

Compound 235 (R)—N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2,3-dihydroxy-propyl)-benzenesulfonamide

MS: m/z 464.0 (MNa⁺).

Compound 236 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-[2-(2-oxo-pyrrolidin-1-yl)-ethyl]-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.84 (p, 2H), 2.14 (t, 2H), 3.29-3.38 (m, 4H), 3.78 (br t, 2H), 7.49-7.58 (m, 2H), 7.66 (t, 2H), 7.72-7.87 (m, 4H), 7.98-8.04 (m, 1H); MS: m/z 479.0 (MH⁺).

Compound 237 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-morpholin-4-yl-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.07-3.20 (m, 2H), 3.32-3.42 (m, 2H), 3.44-3.56 (m, 2H), 3.61-3.78 (m, 2H), 3.88-3.99 (m, 2H), 4.03-4.18 (m, 2H), 7.53-7.60 (m, 2H), 7.69 (t, 2H), 7.76-7.86 (m, 2H), 7.90 (d, 2H), 8.01-8.06 (m, 1H), 10.75 (br s, 1H); MS: m/z 481.0 (MH⁺).

Compound 238 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-dimethylamino-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.85 (s, 6H), 3.33 (br t, 2H), 4.02 (br t, 2H), 7.53-7.60 (m, 2H), 7.69 (t, 2H), 7.75-7.80 (m, 1H), 7.83 (t, 1H), 7.89 (d, 2H), 8.01-8.07 (m, 1H), 9.59 (br s, 1H); MS: m/z 439.1 (MH⁺).

Compound 239 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-methanesulfonyl-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.06 (s, 3H), 3.43 (br t, 2H), 4.05 (br t, 2H), 7.51-7.60 (m, 2H), 7.69 (t, 2H), 7.75-7.85 (m, 2H), 7.88 (dd, 2H), 8.00-8.06 (m, 1H); MS: m/z 495.9 (MNa⁺).

Compound 240 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-[2-(2-oxo-imidazolidin-1-yl)-ethyl]-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.13 (t, 2H), 3.19 (t, 2H), 3.31 (t, 2H), 3.76 (t, 2H), 6.36 (br s, 1H), 7.50-7.58 (m, 2H), 7.66 (t, 2H), 7.72-7.81 (m, 2H), 7.85 (dd, 2H), 7.97-8.04 (m, 1H); MS: m/z 480.0 (MH⁺).

Compound 241 (S)—N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(1-methyl-pyrrolidin-2-ylmethyl)-benzenesulfonamide

MS: m/z 465.0 (MH⁺).

Compound 242 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2,2-difluoro-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.16 (dt, 2H), 6.23 (tt, 1H), 7.50-7.57 (m, 2H), 7.65 (t, 2H), 7.71-7.76 (m, 1H), 7.79 (t, 1H), 7.86 (d, 2H), 7.98-8.04 (m, 1H); MS: m/z 432.1 (MH⁺).

Compound 243 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(carbomethoxymethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.62 (s, 3H), 4.63 (s, 2H), 7.48-7.56 (m, 2H), 7.62 (t, 2H), 7.68-7.72 (m, 1H), 7.75 (t, 1H), 7.84 (dd, 2H), 7.97-8.03 (m, 1H); MS: m/z 440.1 (MH⁺).

Compound 244 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-[2(S)-methyl-2-carbomethoxy-ethyl]-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.17 (d, 3H), 2.60 (q, 1H), 3.46 (s, 3H), 3.75 (br s, 1H), 3.86 (br s, 1H), 7.50-7.58 (m, 2H), 7.66 (t, 2H), 7.72-7.86 (m, 4H), 7.97-8.03 (m, 1H); MS: m/z 468.1 (MH⁺).

Compound 245 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-[2(R)-methyl-2-carbomethoxy-ethyl]-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.17 (d, 3H), 2.60 (q, 1H), 3.46 (s, 3H), 3.74 (br s, 1H), 3.86 (br s, 1H), 7.50-7.57 (m, 2H), 7.66 (t, 2H), 7.73-7.86 (m, 4H), 7.97-8.03 (m, 1H); MS: m/z 468.1 (MH⁺).

Compound 246 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3-phenyl-propyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.71 (p, 2H), 2.65 (br t, 2H), 3.64 (br t, 2H), 7.09-7.19 (m, 3H), 7.23 (t, 2H), 7.50-7.59 (m, 2H), 7.67 (t, 2H), 7.75-7.86 (m, 4H), 7.97-8.03 (m, 1H); MS: m/z 486.1 (MH⁺).

Compound 247 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.08 (t, 3H), 3.66 (q, 2H), 7.50-7.59 (m, 2H), 7.67 (t, 2H), 7.75-7.82 (m, 2H), 7.86 (dd, 2H), 7.98-8.03 (m, 1H); MS: m/z 396.0 (MH⁺).

Compound 248 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(hexyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.81 (t, 3H), 1.11-1.25 (m, 4H), 1.26-1.36 (m, 2H), 1.36-1.46 (m, 2H), 3.59 (br t, 2H), 7.50-7.58 (m, 2H), 7.67 (t, 2H), 7.75-7.82 (m, 2H), 7.85 (d, 2H), 7.97-8.03 (m, 1H); MS: m/z 452.1 (MH⁺).

Compound 249 N-(Adamant-1-ylmethyl)-N-(3-bromo-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.42 (d, 3H), 1.53 (d, 6H), 1.62 (d, 3H), 1.87 (s, 3H), 3.06 (d, 1H), 3.62 (d, 1H), 7.48-7.56 (m, 2H), 7.62 (t, 2H), 7.73-7.80 (m, 4H), 7.94-8.00 (m, 1H); MS: m/z 516.2 (MH⁺).

Compound 250 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.51-2.66 (m, 2H), 3.93 (t, 2H), 7.52-7.58 (m, 2H), 7.66 (t, 2H), 7.74-7.83 (m, 2H), 7.85 (dd, 2H), 8.00-8.04 (m, 1H); MS: m/z 464.0 (MH⁺).

Compound 251 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(pent-3-ynyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.59 (t, 3H), 2.33-2.40 (m, 2H), 3.74 (t, 2H), 7.50-7.57 (m, 2H), 7.66 (t, 2H), 7.74-7.81 (m, 2H), 7.86 (dd, 2H), 7.98-8.03 (m, 1H); MS: m/z 434.0 (MH⁺).

Compound 252 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-methoxy-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.13 (s, 3H), 3.40 (t, 2H), 3.82 (t, 2H), 7.49-7.56 (m, 2H), 7.65 (t, 2H), 7.73-7.80 (m, 2H), 7.85 (d, 2H), 7.97-8.02 (m, 1H); MS: m/z 426.1 (MH⁺).

Compound 253 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-oxo-pentyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.59 (p, 2H), 2.04 (s, 3H), 2.58 (t, 2H), 3.57 (br t, 2H), 7.50-7.58 (m, 2H), 7.67 (t, 2H), 7.75-7.86 (m, 4H), 7.97-8.03 (m, 1H); MS: m/z 452.0 (MH⁺).

Compound 254 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(dimethoxyphosphinoyl-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.02-2.13 (m, 2H), 3.58 (s, 3H), 3.61 (s, 3H), 3.76-3.86 (m, 2H), 7.51-7.58 (m, 2H), 7.68 (t, 2H), 7.74-7.87 (m, 4H), 7.98-8.04 (m, 1H); MS: m/z 504.1 (MH⁺).

Compound 255 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclopropylmethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.06-0.11 (m, 2H), 0.35-0.41 (m, 2H), 0.83-0.95 (m, 1H), 3.52 (dd, 2H), 7.50-7.57 (m, 2H), 7.66 (t, 2H), 7.74-7.80 (m, 2H), 7.83-7.88 (m, 2H), 7.97-8.02 (m, 1H); MS: m/z 422.0 (MH⁺).

Compound 256 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-piperidin-1-yl-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.27-1.38 (m, 1H), 1.50-1.71 (m, 3H), 1.75-1.84 (m, 2H), 2.88-3.01 (m, 2H), 3.26-3.34 (m, 2H), 3.46-3.55 (m, 2H), 3.99-4.08 (m, 2H), 7.53-7.59 (m, 2H), 7.69 (t, 2H), 7.76-7.80 (m, 1H), 7.83 (t, 1H), 7.88 (dd, 2H), 8.01-8.06 (m, 1H), 9.16 (br s, 1H); MS: m/z 479.0 (MH⁺).

Compound 257 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-[2-(2,5-dioxo-pyrrolidin-1-yl)-ethyl]-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.54 (s, 4H), 3.56 (t, 2H), 3.82 (t, 2H), 7.52-7.57 (m, 2H), 7.66 (t, 2H), 7.72-7.81 (m, 4H), 8.01-8.06 (m, 1H); MS: m/z 492.9 (MH⁺).

Compound 258 (R)—N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5-oxo-pyrrolidin-2-ylmethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.87-2.00 (m, 1H), 2.02-2.25 (m, 3H), 3.45-3.75 (m, 3H), 7.46 (br s, 1H), 7.51-7.57 (m, 2H), 7.67 (t, 2H), 7.74-7.83 (m, 2H), 7.86 (d, 2H), 7.98-8.03 (m, 1H); MS: m/z 464.9 (MH⁺).

Compound 259 (S)—N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5-oxo-pyrrolidin-2-ylmethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.85-1.99 (m, 1H), 2.02-2.25 (m, 3H), 3.44-3.76 (m, 3H), 4.76 (br s, 1H), 7.51-7.57 (m, 2H), 7.67 (t, 2H), 7.74-7.83 (m, 2H), 7.86 (d, 2H), 7.98-8.03 (m, 1H); MS: m/z 465.0 (MH⁺).

Compound 260 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-methylsulfanyl-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.02 (s, 3H), 2.62 (t, 2H), 3.83 (t, 2H), 7.51-7.57 (m, 2H), 7.66 (t, 2H), 7.73-7.82 (m, 2H), 7.87 (d, 2H), 7.98-8.04 (m, 1H); MS: m/z 441.9 (MH⁺).

Compound 261 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 0.84 (t, 3H), 1.30-1.41 (m, 5H), 1.47 (p, 2H), 3.38 (q, 2H), 3.69 (t, 2H), 7.51-7.60 (m, 2H), 7.77-7.83 (m, 1H), 7.99-8.05 (m, 1H); MS: m/z 376.0 (MH⁺).

Compound 262 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclopropylmethyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 0.11-0.17 (m, 2H), 0.40-0.46 (m, 2H), 0.92-1.03 (m, 1H), 1.34 (t, 3H), 3.38 (q, 2H), 3.57 (d, 2H), 7.51-7.59 (m, 2H), 7.77-7.83 (m, 1H), 8.00-8.05 (m, 1H); MS: m/z 374.0 (MH⁺).

Compound 263 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2,2-difluoro-ethyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.35 (t, 3H), 3.47 (q, 2H), 4.17 (dt, 2H), 6.22 (tt, 1H), 7.52-7.59 (m, 2H), 7.77-7.83 (m, 1H), 8.01-8.06 (m, 1H); MS: m/z 384.1 (MH⁺).

Compound 264 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-tert-butoxy-ethyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.10 (s, 9H), 1.35 (t, 3H), 3.38-3.47 (m, 4H), 3.81 (t, 2H), 7.50-7.58 (m, 2H), 7.76-7.81 (m, 1H), 7.99-8.06 (m, 1H); MS: m/z 442.0 (MNa⁺).

Compound 265 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-N′,N′-dimethylsulfamide

¹H-NMR (DMSO-d₆): δ 0.84 (t, 3H), 1.34 (h, 2H), 1.45 (p, 2H), 2.89 (s, 6H), 3.58 (t, 2H), 7.50-7.58 (m, 2H), 7.76-7.81 (m, 1H), 7.98-8.04 (m, 1H); MS: m/z 391.0 (MH⁺).

Compound 266 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclopropylmethyl)-N′,N′-dimethylsulfamide

¹H-NMR (DMSO-d₆): δ 0.08-0.14 (m, 2H), 0.37-0.44 (m, 2H), 0.89-1.01 (m, 1H), 2.87 (s, 6H), 3.48 (d, 2H), 7.50-7.57 (m, 2H), 7.76-7.82 (m, 1H), 7.98-8.04 (m, 1H); MS: m/z 389.0 (MH⁺).

Compound 267 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-tert-butoxy-ethyl)-N′,N′-dimethylsulfamide

¹H-NMR (DMSO-d₆): δ 1.08 (s, 9H), 2.91 (s, 6H), 3.42 (t, 2H), 3.72 (t, 2H), 7.49-7.56 (m, 2H), 7.75-7.80 (m, 1H), 7.98-8.03 (m, 1H); MS: m/z 435.1 (MH⁺).

Compound 268 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2,2-difluoro-ethyl)-N′,N′-dimethylsulfamide

¹H-NMR (DMSO-d₆): δ 2.89 (s, 6H), 4.07 (dt, 2H), 6.21 (tt, 1H), 7.51-7.58 (m, 2H), 7.76-7.82 (m, 1H), 8.00-8.06 (m, 1H); MS: m/z 399.0 (MH⁺).

Compound 269 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoropropyl)-N′,N′-dimethylsulfamide

¹H-NMR (DMSO-d₆): δ 2.54-2.68 (m, 2H), 2.89 (s, 6H), 3.87 (t, 2H), 7.52-7.59 (m, 2H), 7.77-7.84 (m, 1H), 8.01-8.07 (m, 1H); MS: m/z 431.0 (MH⁺).

Example 22

Compound 270 N-(2-Amino-ethyl)-N-(3-chloro-benzo[b]thiophen-2-yl)-benzenesulfonamide

To compound 86 (0.035 g, 0.075 mmol), dissolved in CH₂Cl₂ (1 mL), was added trifluoroacetic acid (1 mL) and the reaction mixture was stirred at room temperature for 3 h. The reaction mixture was evaporated in vacuo, and the residue triturated with hexanes (2 mL) to afford compound 270 as a brown solid (0.031 g, 86%). ¹H-NMR (CDCl₃): δ 3.17-3.28 (t, 2H), 3.58-3.62 (t, 2H), 7.34-7.55 (m, 4H), 7.58-7.70 (m, 5H); MS: m/z 367.1 (MH⁺).

Example 23

Compound 271 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-carboxy-benzenesulfonamide

To a solution of Ph₃P (0.888 g, 3.39 mmol) in THF (27 mL) was added a solution of DEAD (1.50 mL, 3.38 mmol). After stirring for 2 min, compound 271-A (0.782 g, 2.25 mmol) was added. To a portion (0.25 mmol of 271-A) of the aforementioned reaction mixture was added 3,3,3-trifluoropropan-1-ol (0.025 mL, 0.30 mmol). The reaction was stirred for 2 days, 1N NaOH (0.5 mL, 0.5 mmol) was added, and the reaction was evaporated in vacuo. The crude residue was re-dissolved in 1:1 dichloroethane/acetic acid (2 mL), and NBS (0.053 g, 0.30 mmol) was added. After stirring overnight an additional portion of NBS (0.041 g, 0.23 mmol) was added, and the reaction stirred for an additional 4 h. The reaction mixture was evaporated in vacuo and purified by reverse-phase chromatography (25-95% acetonitrile/water+0.1% TFA) to afford compound 271 as a tan powder (0.069 g, 0.14 mmol). ¹H-NMR (DMSO-d₆): δ 2.54-2.68 (m, 2H), 3.98 (t, 2H), 7.52-7.59 (m, 2H), 7.73-7.79 (m, 1H), 7.97 (d, 2H), 8.00-8.06 (m, 1H), 8.16 (d, 2H), 13.60 (br s, 1H); MS: m/z 507.9 (MH⁺).

Following the procedure described above for example 23 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared.

Compound 272 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.83 (t, 3H), 1.30-1.47 (m, 4H), 3.65 (br t, 2H), 7.50-7.58 (m, 2H), 7.75-7.80 (m, 1H), 7.96 (d, 2H), 7.99-8.03 (m, 1H), 8.17 (d, 2H), 13.58 (s, 1H); MS: m/z 468.0 (MH⁺).

Compound 273 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclopropylmethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.06-0.15 (m, 2H), 0.36-0.43 (m, 2H), 0.85-0.97 (m, 1H), 3.56 (d, 2H), 7.50-7.58 (m, 2H), 7.74-7.80 (m, 1H), 7.97 (d, 2H), 7.99-8.03 (m, 1H), 8.16 (d, 2H), 13.58 (br s, 1H); MS: m/z 465.9 (MH⁺).

Compound 274 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-methoxyethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 3.14 (s, 3H), 3.41 (t, 2H), 3.87 (t, 2H), 7.50-7.57 (m, 2H), 7.72-7.78 (m, 1H), 7.96 (d, 2H), 7.99-8.03 (m, 1H), 8.15 (d, 2H), 13.57 (s, 1H); MS: m/z 470.0 (MH⁺).

Compound 275 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-tert-butoxy-ethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.98 (s, 9H), 3.42 (t, 2H), 3.84 (t, 2H), 7.49-7.56 (m, 2H), 7.71-7.78 (m, 1H), 7.95-8.03 (m, 3H), 8.15 (d, 2H), 13.56 (br s, 1H); MS: m/z 512.0 (MH⁺).

Compound 276 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2,2-difluoro-ethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ: 4.19 (dt, 2H), 6.24 (tt, 1H), 7.51-7.58 (m, 2H), 7.71-7.77 (m, 1H), 7.98 (d, 2H), 8.01-8.05 (m, 1H), 8.15 (d, 2H), 13.61 (s, 1H); MS: m/z 475.9 (MH⁺).

Compound 277 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-morpholin-4-yl-ethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CD₃OD): δ 3.38 (br s, 4H), 3.46 (t, 2H), 3.91 (br s, 4H), 4.20 (t, 2H), 7.49-7.56 (m, 2H), 7.76-7.82 (m, 1H), 7.84-7.90 (m, 1H), 7.97 (d, 2H), 8.23 (d, 2H); MS: m/z 525.0 (MH⁺).

Compound 278 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(adamant-1-yl-methyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.40-1.48 (m, 3H), 1.50-1.58 (m, 6H), 1.58-1.66 (m, 3H), 1.88 (br s, 3H), 3.12 (d, 1H), 3.65 (d, 1H), 7.48-7.56 (m, 2H), 7.74-7.79 (m, 1H), 7.88 (d, 2H), 7.96-8.01 (m, 1H), 8.13 (d, 2H), 13.57 (s, 1H); MS: m/z 560.0 (MH⁺).

Compound 279 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclohexylmethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.89-1.02 (m, 2H), 1.02-1.19 (m, 3H), 1.25-1.38 (m, 1H), 1.52-1.60 (m, 1H), 1.60-1.94 (m, 4H), 3.49 (br s, 2H), 7.50-7.58 (m, 2H), 7.73-7.80 (m, 1H), 7.94 (d, 2H), 7.97-8.03 (m, 1H), 8.15 (d, 2H), 13.58 (br s, 1H); MS: m/z 508.0 (MH⁺).

Compound 390 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(ethyl)-4-carboxy-benzenesulfonamide

MS: m/z 438.1 (M-H)⁻.

Compound 391 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(propyl)-4-carboxy-benzenesulfonamide

MS: m/z 452.1 (M-H)⁻.

Compound 392 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(pentyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.80 (t, 3H), 1.37-1.15 (m, 4H), 1.50-1.38 (m, 2H), 3.64 (t, 2H), 7.59-7.50 (m, 2H), 7.81-7.74 (m, 1H), 8.03-7.93 (m, 3H), 8.17 (d, 2H), 13.59 (s, 1H); MS: m/z 480.1 (M-H)⁻.

Compound 393 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(hexyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.81 (t, 3H), 1.25-1.12 (m, 4H), 1.49-1.26 (m, 4H), 3.64 (t, 2H), 7.59-7.50 (m, 2H), 7.81-7.74 (m, 1H), 8.04-7.94 (m, 3H), 8.17 (d, 2H), 13.59 (s, 1H); MS: m/z 494 (M-H)⁻.

Compound 394 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.76-1.64 (m, 2H), 2.48-2.34 (m, 2H), 3.74 (t, 2H), 7.60-7.51 (m, 2H), 7.82-7.76 (m, 1H), 7.97 (d, 2H), 8.06-8.00 (m, 1H), 8.18 (d, 2H), 13.62 (s, 1H); MS: m/z 520 (M-H)⁻.

Compound 395 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.65-1.46 (m, 4H), 2.34-2.14 (m, 2H), 3.68 (br t, 2H), 7.59-7.50 (m, 2H), 7.82-7.74 (m, 1H), 8.04-7.95 (m, 3H), 8.17 (d, 2H), 13.59 (s, 1H); MS: m/z 534.1 (M-H)⁻.

Compound 396 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-cyclopropylethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.03-0.04 (m, 2H), 0.39-0.31 (m, 2H), 0.81-0.68 (m, 1H), 1.39 (q, 2H), 3.72 (t, 2H), 7.58-7.49 (m, 2H), 7.79-7.74 (m, 1H), 8.03-7.94 (m, 3H), 8.17 (d, 2H), 13.59 (s, 1H); MS: m/z 478.1 (M-H)⁻.

Compound 397 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3-tert-butoxypropyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.06 (s, 9H), 1.60 (p, 2H), 3.32 (t, 2H), 3.71 (br t, 2H), 7.59-7.49 (m, 2H), 7.81-7.75 (m, 1H), 7.96 (d, 2H), 8.04-7.98 (m, 1H), 8.17 (d, 2H), 13.59 (br s, 1H); MS: m/z 524 (M-H)⁻.

Compound 437 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclobutylmethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.71-1.60 (m, 2H), 1.83-1.72 (m, 2H), 1.95-1.85 (m, 2H), 2.40-2.31 (m, 1H), 3.68 (br s, 2H), 7.57-7.50 (m, 2H), 7.79-7.73 (m, 1H), 8.02-7.94 (m, 3H), 8.17 (d, 2H), 13.59 (s, 1H); MS: m/z 478 (M-H)⁻.

Compound 438 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclopentylmethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.29 (br s, 2H), 1.49-1.39 (m, 2H), 1.60-1.50 (m, 2H), 1.73-1.60 (br m, 2H), 1.89 (p, 1H), 3.73-334 (br m, 2H), 7.58-7.50 (m, 2H), 7.79-7.74 (m, 1H), 7.95 (d, 2H), 8.02-7.97 (m, 1H), 8.16 (d, 2H), 13.59 (s, 1H); MS: m/z 492.2 (M-H)⁻.

Compound 439 RS,RS—N-(Bicyclo[2.2.1]heptan-2-ylmethyl)-N-(3-bromobenzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.21-0.62 (m, 11H), 3.63 (br s, 2H), 7.58-7.49 (m, 2H), 7.80-7.74 (m, 1H), 8.02-7.93 (m, 3H), 8.18-8.13 (m, 2H), 13.59 (br s, 1H); MS: m/z 518.2 (M-H)⁻.

Compound 440 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-((tetrahydro-2H-pyran-4-yl)methyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.23 (m, 2H), 1.84-1.52 (m, 3H), 3.23-3.13 (m, 2H), 3.55 (br s, 2H), 3.85-3.76 (m, 2H), 7.58-7.50 (m, 2H), 7.80-7.74 (m, 1H), 7.95 (d, 2H), 8.03-7.98 (m, 1H), 8.16 (d, 2H), 13.59 (s, 1H); MS: m/z 508.1 (M-H)⁻.

Compound 441 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-(dimethylamino)ethyl)-4-carboxy-benzenesulfonamide

MS: m/z 481 (M-H)⁻.

Compound 452 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(isobutyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.93 (d, 6H), 1.66-1.54 (m, 1H), 3.38 (br s, 2H), 7.57-7.50 (m, 2H), 7.79-7.74 (m, 1H), 7.94 (d, 2H), 8.02-7.97 (m, 1H), 8.15 (d, 2H), 13.58 (s, 1H); MS: m/z 466.1 (M-H)⁻.

Compound 453 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-(cyclohexyloxy)ethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.16-0.97 (m, 5H), 1.42-1.33 (m, 1H), 1.56-1.47 (m, 2H), 1.66-1.57 (m, 2H), 3.14-3.07 (m, 1H), 3.46 (t, 2H), 3.86 (t, 2H), 7.56-7.49 (m, 2H), 7.78-7.73 (m, 1H), 8.03-7.96 (m, 3H), 8.15 (d, 2H), 13.55 (s, 1H); MS: m/z 536.2 (M-H)⁻.

Compound 454 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3-methoxy-3-methylbutyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.05 (s, 6H), 1.72-1.65 (m, 2H), 2.98 (s, 3H), 3.73-3.64 (m, 2H), 7.58-7.51 (m, 2H), 7.80-7.75 (m, 1H), 7.97 (d, 2H), 8.03-7.99 (m, 1H), 8.18 (d, 2H), 13.59 (s, 1H); MS: m/z 510.2 (M-H)⁻.

Compound 523 N-(3-Methyl-benzo[b]thiophen-2-yl)-N—(C-benzo[1,3]dioxol-5-yl-methy)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.82-2.03 (m, 3H), 4.67 (br s, 2H), 5.97 (s, 2H), 6.67 (dd, 1H), 6.78 (d, 2H), 7.25-7.44 (m, 2H), 7.61-7.73 (m, 1H), 7.73-7.88 (m, 1H), 7.98 (m, 2H), 8.17 (m, 2H), 13.60 (br s, 1H); MS: m/z 504.0 (MH⁺).

Compound 524 N-(3-Methyl-benzo[b]thiophen-2-yl)-N—(C-(2,2-difluoro-benzo[1,3]dioxol-5-yl)-methyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.95 (s, 3H), 4.81 (br s, 2H), 7.11 (dd, 1H), 7.22-7.48 (m, 4H), 7.57-7.73 (m, 1H), 7.76-7.92 (m, 1H), 7.99 (m, 2H), 8.18 (m, 2H), 13.61 (br s, 1H); MS: m/z 540.0 (MH⁺).

Compound 525 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,4-dimethoxy-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.97 (s, 3H), 3.31 (s, 4H), 3.62-3.75 (m, 3H), 4.66 (br s, 1H), 6.61-6.74 (m, 1H), 6.74-6.89 (m, 2H), 7.25-7.44 (m, 2H), 7.61-7.72 (m, 1H), 7.72-7.85 (m, 1H), 7.99 (m, 2H), 8.18 (m, 2H), 13.59 (s, 1H); MS: m/z 520.0 (MH⁺).

Example 24

Compound 280 N-(Butyl)-N-[3-(1-hydroxy-ethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

To a solution of Ph₃P (0.494 g, 1.88 mmol) in THF (15 mL) was added a solution of DEAD (0.84 mL, 1.89 mmol). After stirring for a few minutes, compound 205-B (0.354 g, 1.25 mmol) was added. To a portion of the aforementioned reaction mixture (0.25 mmol of 205-B) was added n-butan-1-ol (0.027 mL, 0.30 mmol) and the reaction stirred for 2 days. Methanol (0.50 mL) was added followed by NaBH₄ (0.019 g, 0.50 mmol) and the reaction was stirred for 3 h. The reaction mixture was evaporated in vacuo and purified by reverse-phase chromatography (25-95% acetonitrile/water+0.1% TFA) to afford compound 280 as a tan semi-solid (0.053 g, 0.16 mmol). ¹H-NMR (DMSO-d₆): δ 0.86 (t, 3H), 1.22-1.37 (m, 5H), 1.44-1.57 (m, 5H), 3.26-3.41 (m, 2H), 3.46 (br s, 1H), 3.70 (br s, 1H), 5.09-5.18 (br d, 1H), 5.26 (br s, 1H), 7.37-7.43 (m, 2H), 7.87-7.93 (m, 1H), 8.22-8.27 (m, 1H); MS: m/z 364.0 (MH⁺).

Following the procedure described above for example 24 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared.

Compound 281 N-(Cyclopropylmethyl)-N-(3-(1-hydroxyethyl)benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 0.15-0.26 (m, 2H), 0.48 (d, 2H), 1.01 (br s, 1H), 1.30 (t, 3H), 1.54 (d, 3H), 3.26-3.39 (m, 2H), 3.39-3.57 (m, 2H), 5.17-5.27 (m, 2H), 7.37-7.43 (m, 2H), 7.39-7.88 (m, 1H), 8.22-8.28 (m, 1H); MS: m/z 362.1 (MNa⁺).

Compound 282 N-(3-(1-Hydroxyethyl)benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.30 (t, 3H), 1.54 (d, 3H), 2.57-2.73 (m, 2H), 3.32-3.53 (m, 2H), 3.67 (br s, 1H), 4.07 (br s, 1H), 5.10 (br s, 1H), 5.34 (br s, 1H), 7.40-7.46 (m, 2H), 7.91-7.96 (m, 1H), 8.23-8.29 (m, 1H); MS: m/z 404.1 (MNa⁺).

Compound 283 N-(2-tert-Butoxyethyl)-N-(3-(1-hydroxyethyl)benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (DMSO-d₆): δ 1.16 (s, 9H), 1.31 (t, 3H), 1.53 (d, 3H), 3.36-3.52 (m, 4H), 3.73 (m, 2H), 5.11 (br s, 1H), 5.30 (br s, 1H), 7.37-7.44 (m, 2H), 7.88-7.93 (m, 1H), 8.21-8.26 (m, 1H); MS: m/z 408.1 (MNa⁺).

Compound 284 N-(3-(1-Hydroxyethyl)benzo[b]thiophen-2-yl)-N-(2-morpholinoethyl)-ethanesulfonamide

MS: m/z 399.1 (MH⁺).

Example 25

Compound 285 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-hydroxy-benzenesulfonamide

A solution of boron tribromide (1.0 M in dichlorormethane, 1.57 mL, 1.57 mmol) was added to a solution of compound 26 (180 mg, 0.392 mmol) in dichloromethane (10 mL), at 0° C. The resultant solution was stirred at 0° C. for 1 h, then treated with 2 N hydrochloric acid. The organic layer was separated, dried over sodium sulfate, filtered, and the solvent evaporated in vacuo. The residue was purified by HPLC (C₁₈) eluting with an acetonitrile-water (0.1% TFA) gradient (40-90%). The resulting residue was further purified by flash column chromatography (SiO₂), eluting with an ethyl acetate-heptane gradient to afford compound 285 as a colorless solid (33 mg, 19%). ¹H-NMR (DMSO-d₆): δ 1.98 (s, 3H), 4.67 (br s, 2H), 6.96 (d, 2H), 7.11-7.14 (m, 1H), 7.25-7.40 (m, 4H), 7.64-7.68 (m, 3H), 7.80-7.85 (m, 1H), 10.73 (br s, 1H); MS: m/z 446.1 (MH⁺).

Following the procedure described above for example 25 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared.

Compound 286 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-hydroxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.97 (s, 3H), 4.71 (s, 2H), 7.09-7.17 (m, 3H), 7.26-7.40 (m, 5H), 7.49 (t, 1H), 7.65-7.70 (m, 1H), 7.81-7.86 (m, 1H), 10.24 (br s, 1H); MS: m/z 446.1 (MH⁺).

Compound 287 N-(Benzo[b]thiophen-2-yl)-N-(3-hydroxy-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.75 (s, 2H), 6.69-6.71 (m, 1H), 6.85-6.87 (m, 2H) 7.01 (s, 1H), 7.10-7.14 (t, 1H), 7.26-7.29 (m, 2H), 7.48-7.52 (m, 2H), 7.60-7.63 (m, 3H), 7.76-7.78 (d, 2H); MS: m/z 396.0 (MH⁺).

Compound 288 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-hydroxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.83 (s, 2H), 6.97-6.99 (d, 2H), 7.40-7.51 (m, 3H), 7.63-7.73 (m, 5H), 7.96-7.98 (m, 1H), 10.76 (s, 1H); MS: m/z 516.0 (MH⁺).

Compound 289 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-hydroxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.88 (s, 2H), 7.15-7.22 (m, 2H), 7.35-7.52 (m, 4H), 7.63-7.73 (m, 3H), 7.97-8.01 (m, 1H), 10.27 (s, 1H); MS: m/z 516.0 (MH⁺).

Compound 290 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-hydroxy-benzenesulfonamide

¹H NMR (DMSO-d₆): δ 4.83 (s, 2H), 6.96-6.99 (d, 2H), 7.37-7.52 (m, 3H), 7.60-7.74 (m, 5H), 7.95-7.98 (m, 1H), 10.75 (s, 1H); MS: m/z 561.9 (MH⁺), 584.0 (MNa⁺).

Compound 291 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-hydroxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.87 (s, 2H), 7.14-7.23 (m, 2H), 7.35-7.52 (m, 5H), 7.59-7.71 (m, 3H), 7.96-7.99 (m, 1H), 10.26 (s, 1H); MS: m/z 561.9 (MH⁺).

Compound 780 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-hydroxy-4-methanesulfonylamino-benzenesulfonamide

MS: m/z 608.89 (MH⁺).

Example 26

Compound 292 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

To a solution of compound 192 (87.1 mg, 0.145 mmol) in MeOH (2 mL) was added 3N NaOH (73 μL, 0.218 mmol) and the reaction was refluxed for 18 h. The reaction was cooled to ambient temperature and the solvent evaporated under reduced pressure. The residue was dissolved in H₂O, cooled to 0° C., and acidified with 1N HCl. The precipitate was filtered, washed extensively with H₂O, and dried under vacuo to afford compound 292 as a white solid (0.063 g, 74%). ¹H-NMR (CD₃OD): δ 4.94 (s, 2H), 7.16-7.21 (t, 1H), 7.42-7.46 (m, 2H), 7.52-7.56 (m, 1H), 7.61-7.63 (m, 1H), 7.68-7.70 (m, 1H), 7.75-7.77 (m, 1H), 7.99-8.01 (d, 2H), 8.22-8.25 (d, 2H); MS: m/z 588.0 (MH⁺).

Following the procedure described above for example 26 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 293 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carboxy-benzenesulfonamide

¹H-NMR (CD₃OD): δ 4.93 (s, 2H), 7.16-7.21 (t, 1H), 7.42-7.45 (m, 2H), 7.45-7.52 (m, 1H), 7.53-7.56 (m, 1H), 7.60-7.79 (m, 3H), 8.08-8.10 (d, 1H), 8.34-8.36 (d, 1H), 8.48 (s, 1H); MS: m/z 588.0 (MH⁺).

Compound 294 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.95 (s, 2H), 7.42-7.53 (m, 3H), 7.65-7.74 (m, 3H), 7.97-7.99 (m, 2H), 8.03-8.05 (m, 2H), 8.18-8.20 (m, 1H), 13.64 (s, 1H); MS: m/z 544.0 (MH⁺).

Compound 295 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 5.01 (s, 2H), 7.20 (s, 1H), 7.31-7.35 (m, 2H), 7.45-7.50 (t, 1H), 7.69-7.73 (m, 3H), 7.78-7.85 (m, 2H), 8.05-8.08 (m, 1H), 8.25-8.30 (m, 2H), 13.59 (s, 1H); MS: m/z 510.0 (MH⁺).

Compound 296 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 5.01 (s, 2H), 7.19 (s, 1H), 7.30-7.35 (m, 2H), 7.45-7.50 (t, 1H), 7.69-7.73 (m, 3H), 7.82-7.84 (m, 2H), 7.94-7.96 (m, 2H), 8.15-8.17 (m, 2H), 13.60 (s, 1H); MS: m/z 510.0 (MH⁺).

Compound 297 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 5.06 (s, 2H), 7.42-7.53 (m, 3H), 7.61-7.82 (m, 7H), 7.95-7.99 (m, 1H), 13.81 (s, 1H); MS: m/z 543.9 (MH⁺).

Compound 298 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 5.08 (s, 2H), 7.40-7.51 (m, 3H), 7.59-7.81 (m, 7H), 7.95-7.98 (m, 1H), 13.86 (s, 1H); MS: m/z 590.0 (MH⁺).

Compound 299 N-(3-Formyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 5.08 (br s, 2H), 7.42-7.54 (m, 3H), 7.69-7.80 (m, 2H), 7.97-8.04 (m, 3H), 8.20 (d, 2H), 8.42-8.47 (m, 1H), 9.85 (s, 1H), 13.70 (br s, 1H); MS: m/z 538.2 (MH⁺).

Compound 305 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.96 (s, 3H), 3.89 (s, 3H), 4.88 (br s, 2H), 7.38-7.42 (m, 3H), 7.69-7.72 (m, 1H), 7.84-7.88 (m, 2H), 8.16-8.18 (m, 1H), 8.27-8.28 (t, 1H), 8.33-8.35 (m, 1H).

Compound 306 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.00 (s, 3H), 4.89 (s, 2H), 7.40-7.45 (m, 2H), 7.47-7.52 (m, 1H), 7.68-7.74 (m, 3H), 7.80-7.82 (d, 2H), 7.87-7.90 (m, 1H), 8.09-8.11 (d, 2H); MS: m/z 524.0 (MH⁺).

Compound 307 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.95 (s, 2H), 7.41-7.55 (m, 3H), 7.64-7.76 (m, 3H), 7.82-7.86 (m, 1H), 7.97-8.00 (m, 1H), 8.16-8.19 (m, 1H), 8.31-8.34 (m, 2H), 13.61 (s, 1H); MS: m/z 543.9 (MH⁺).

Compound 318 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.38 (s, 3H), 5.00 (s, 2H), 7.42-7.50 (m, 3H), 7.68-7.75 (m, 2H), 7.93-7.97 (m, 3H), 8.01-8.05 (m, 1H), 8.18 (d, 2H); MS: m/z 552.2 (MH⁺).

Compound 376 N-(6-Fluoro-3-methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.94 (s, 3H), 4.87 (s, 2H), 7.23-7.35 (m, 1H), 7.42-7.49 (m, 1H), 7.61-7.86 (m, 5H), 8.12-8.15 (d, 1H), 8.27-8.33 (m, 2H), 13.61 (s, 1H); MS: m/z 542.0 (MH⁺).

Compound 423 N-(Butyl)-N-(3-methoxy-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.83 (t, 3H), 1.26-1.38 (m, 2H), 1.42-1.52 (m, 2H), 3.56 (t, 2H), 3.97 (s, 3H), 7.39-7.46 (m, 2H), 7.75-7.84 (m, 2H), 7.96 (d, 2H), 8.15 (d, 2H), 13.58 (br s, 1H); MS: m/z 420.1 (MH⁺).

Compound 426 N-(6-Fluoro-3-methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.65-1.69 (m, 2H), 2.21 (s, 3H), 2.30-2.40 (m, 2H), 3.66 (m, 2H), 7.30-7.35 (m, 1H), 7.81-7.84 (m, 2H), 7.85-7.91 (m, 2H), 8.15-8.17 (d, 1H), 13.62 (s, 1H); MS: m/z 476.0 (MH⁺).

Compound 427 N-(6-Fluoro-3-methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.91 (s, 3H), 4.89 (s, 2H), 7.22-7.27 (m, 1H), 7.42-7.47 (t, 1H), 7.63-7.80 (m, 6H), 8.03-8.05 (d, 1H), 13.62 (s, 1H); MS: m/z 542.0 (MH⁺).

Compound 432 N-(Butyl)-N-(1,1-dioxo-1H-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.87 (t, 3H), 1.16-1.41 (m, 2H), 1.49-1.67 (m, 2H), 3.72 (t, 2H), 7.56-7.76 (m, 4H), 7.80 (d, 1H), 8.01 (d, 2H), 8.12 (d, 2H); MS: m/z 422.1 (MH⁺).

Compound 450 N-(6-Fluoro-3-methyl-benzo[b]thiophen-2-yl)-N-(butyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.828-0.864 (t, 3H), 1.28-1.44 (m, 4H), 2.22 (s, 3H), 3.51-3.56 (m, 2H), 7.28-7.33 (m, 1H), 7.79-7.82 (m, 2H), 7.83-7.90 (m, 2H), 8.13-8.15 (m, 2H), 13.62 (s, 1H); MS: m/z 422.1 (MH⁺).

Compound 451 N-(Benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-carboxy-benzenesulfonamide

MS: m/z 444.0 (MH⁺).

Compound 456 N-(Benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-carboxy-benzenesulfonamide

MS: m/z 430.0 (MH⁺).

Compound 468 N-(Butyl)-N-(3-carbamoyl-benzo[b]thiophen-2-yl)-4-carboxy-benzene sulfonamide

MS: m/z 433.0 (MH⁺).

Compound 469 N-(Butyl)-N-(3-dimethylcarbamoyl-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

MS: m/z 461.1 (MH⁺).

Compound 486 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃) δ 1.98 (s, 3H), 3.50 (br s, 2H), 7.24 (d, 5H), 7.29-7.40 (m, 2H), 7.52-7.61 (m, 1H), 7.61-7.70 (m, 1H), 7.95 (m, 2H), 8.26 (m, 2H); MS: m/z 452.5 (MH⁺).

Compound 487 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃) δ 1.98 (s, 3H), 3.50 (br s, 2H), 6.83-7.00 (m, 2H), 7.20-7.25 (m, 2H), 7.30-7.40 (m, 2H), 7.55-7.69 (m, 2H), 7.94 (m, 2H), 8.26 (m, 2H); MS: m/z 456.0 (MH⁺).

Compound 488 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,4-difluoro-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.00-2.09 (m, 3H), 4.67 (br s, 1H), 6.91-7.08 (m, 2H), 7.08-7.21 (m, 1H), 7.31-7.43 (m, 2H), 7.53-7.71 (m, 2H), 7.94 (m, 2H), 8.27 (m, 2H); MS: m/z 474.0 (MH⁺).

Compound 489 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-chloro-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.06 (s, 3H), 4.67 (br s, 1H), 7.00 (t, 1H), 7.12 (m, 1H), 7.30-7.44 (m, 3H), 7.54-7.71 (m, 2H), 7.94 (m, 2H), 8.27 (m, 2H); MS: m/z 490.0 (MH⁺).

Compound 490 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-difluoromethoxy-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.00 (s, 3H), 4.71 (br s, 2H), 6.2-6.7 (m, 1H), 6.99 (d, 2H), 7.24-7.26 (m, 2H), 7.30-7.44 (m, 2H), 7.52-7.74 (m, 2H), 7.95 (m, 2H), 8.27 (m, 2H); MS: m/z 504.0 (MH⁺).

Compound 491 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.04 (s, 3H), 4.77 (br s, 2H), 7.31-7.40 (m, 3H), 7.44 (d, 1H), 7.51 (d, 1H), 7.54-7.62 (m, 2H), 7.62-7.68 (m, 1H), 7.95 (m, 2H), 8.28 (m, 2H); MS: m/z 506.1 (MH⁺).

Compound 492 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-methylsulfone-benzyl)-4-carboxy-benzenesulfonamide

MS: m/z 538.0 (MH⁺).

Compound 493 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2,3,4,5,6-pentafluoro-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.03-2.20 (m, 3H), 3.50 (br s, 2H), 7.31-7.45 (m, 2H), 7.58-7.73 (m, 2H), 7.95 (m, 2H), 8.26 (m, 2H); MS: m/z 528.0 (MH⁺).

Compound 494 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethylsulfone-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.00 (s, 3H), 3.50 (br s, 2H), 7.30-7.46 (m, 2H), 7.51-7.72 (m, 4H), 7.94 (dd, 4H), 8.15-8.33 (m, 2H); MS: m/z 570.0 (MH⁺).

Compound 495 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(pyridin-3-ylmethyl)-4-carboxy-benzenesulfonamide

MS: m/z 439.0 (MH⁺).

Compound 496 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃) δ 1.98 (s, 3H), 4.70 (br s, 2H), 7.27-7.33 (m, 2H), 7.33-7.40 (m, 2H), 7.53-7.64 (m, 1H), 7.64-7.72 (m, 1H), 7.95 (m, 2H), 8.27 (m, 2H); MS: m/z 522.0 (MH⁺). Anal. (C₂₄H₁₇F₃NO₅S₂.Na.H₂O) C, H, N, F, S, Na, KF.

Compound 497 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3-fluoro-4-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.10 (s, 3H), 4.74 (br s, 2H), 7.12-7.23 (m, 2H), 7.32-7.44 (m, 2H), 7.50 (t, 1H), 7.57-7.72 (m, 2H), 7.94 (m, 2H), 8.28 (m, 2H); MS: m/z 524.0 (MH⁺).

Compound 502 N-(3-Cyclopentyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.69 (s, 1H), 1.25-1.63 (m, 3H), 1.63-1.91 (m, 4H), 3.05 (d, 1H), 4.35 (d, 1H), 5.24 (d, 1H), 7.13-7.48 (m, 3H), 7.49-7.70 (m, 3H), 7.75-7.87 (m, 1H), 7.97 (d, 2H), 8.13 (d, 2H); MS: m/z 578.1 (MH⁺).

Compound 517 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,4,5-trifluoro-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 2.00 (s, 3H), 4.80 (br s, 2H), 7.25 (dd, 2H), 7.34-7.49 (m, 2H), 7.70 (dd, 1H), 7.78-7.91 (m, 1H), 7.99 (m, 2H), 8.18 (m, 2H), 13.62 (s, 1H); MS: m/z 492.5 (MH⁺).

Compound 518 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.94 (s, 3H), 4.89 (br s, 2H), 7.24-7.46 (m, 2H), 7.52 (d, 2H), 7.61-7.78 (m, 3H), 7.83 (dd, 1H), 8.00 (m, 2H), 8.18 (m, 2H), 13.61 (s, 1H); MS: m/z 506.1 (MH⁺).

Compound 519 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2-fluoro-5-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.92 (s, 3H), 4.96 (br s, 2H), 7.33-7.44 (m, 3H), 7.58-7.64 (m, 1H), 7.64-7.70 (m, 1H), 7.76 (br. s., 1H), 7.80-7.92 (m, 1H), 8.00 (m, 2H), 8.19 (m, 2H), 13.62 (s, 1H); MS: m/z 524.0 (MH⁺).

Compound 520 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2,5-dichloro-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.94 (s, 3H), 4.93 (br s, 2H), 7.22-7.51 (m, 5H), 7.62-7.75 (m, 1H), 7.75-7.91 (m, 1H), 7.99 (m, 2H), 8.18 (m, 2H), 13.62 (br s, 1H); MS: m/z 528.0 (MH⁺).

Compound 521 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-chloro-3-fluoro-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.97 (s, 3H), 4.80 (br s, 2H), 7.18 (dd, 1H), 7.30 (dd, 1H), 7.38 (dd, 2H), 7.54 (t, 1H), 7.62-7.76 (m, 1H), 7.76-7.91 (m, 1H), 7.99 (d, 2H), 8.18 (d, 2H), 13.62 (br s, 1H); MS: m/z 490.0 (MH⁺).

Compound 522 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-2-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.87 (s, 3H), 4.99 (br s, 2H), 7.23-7.45 (m, 2H), 7.45-7.75 (m, 4H), 7.75-7.93 (m, 1H), 7.99 (m, 2H), 8.18 (m, 2H), 13.63 (br s, 1H); MS: m/z 524.0 (MH⁺).

Compound 526 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethylsulfanyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.90 (s, 3H), 4.85 (br s, 2H), 7.32-7.46 (m, 4H), 7.65 (d, 3H), 7.73-7.89 (m, 1H), 7.99 (m, 2H), 8.18 (m, 2H), 13.60 (s, 1H); MS: m/z 538.0 (MH⁺).

Compound 527 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-thien-2-ylsulfonamide

¹H-NMR (DMSO-d₆) δ 2.02 (s, 4H), 4.93 (br s, 2H), 7.35-7.51 (m, 4H), 7.58-7.79 (m, 4H), 7.79-7.95 (m, 1H), 8.04 (d, 1H), 8.74 (d, 1H), 13.36 (s, 1H); MS: m/z 530.0 (MH⁺).

Compound 528 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-(5-carboxy-3-methyl-thien-2-yl)-sulfonamide

¹H-NMR (DMSO-d₆) δ 2.01 (s, 3H), 2.19 (s, 3H), 4.94 (br s, 2H), 7.28-7.54 (m, 3H), 7.54-7.80 (m, 4H), 7.80-8.03 (m, 1H), 13.91 (br s, 1H); MS: m/z 544.0 (MH⁺).

Compound 529 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-5-carboxy-furan-2-yl-sulfonamide

MS: m/z 514.0 (MH⁺).

Compound 556 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-4-carboxy-benzenesulfonamide

MS m/z 390.0 (MH⁺).

Compound 557 N-(3-Methyl-6-trifluoromethyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (CD₃OD): δ 2.03 (s, 3H), 7.19-7.24 (t, 1H), 7.53-7.55 (m, 3H), 7.80-7.82 (d, 1H), 7.95-7.98 (d, 2H), 8.09 (s, 1H), 8.23-8.25 (d, 2H).

Compound 558 N-(3-Methyl-6-trifluoromethyl-benzo[b]thiophen-2-yl)-N-(butyl)-4-carboxy-benzenesulfonamide

MS: m/z 472.0 (MH⁺).

Compound 566 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-isopropyl-benzo[b]thiophen-2-371)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.78 (d, 3H), 1.43 (d, 3H), 3.28 (q, 1H), 4.17 (d, 1H), 5.24 (d, 1H), 7.07 (t, 1H), 7.27-7.38 (m, 2H), 7.38-7.46 (m, 1H), 7.59 (dd, 1H), 7.62-7.71 (m, 1H), 7.85-7.93 (m, 1H), 7.98 (d, 2H), 8.30 (d, 2H).

Compound 567 N-(2-Cyclopropyl-ethyl)-N-(3-isopropyl-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ −0.08-0.07 (m, 2H), 0.37-0.49 (m, 2H), 0.57-0.74 (m, 1H), 1.19 (m, 1H), 1.42 (d, 3H), 1.52 (d, 3H), 1.57-1.72 (m, 1H), 3.18-3.32 (m, 1H), 3.55-3.69 (m, 1H), 3.87-4.08 (m, 1H), 7.29-7.40 (m, 2H), 7.63-7.71 (m, 1H), 7.95 (d, 2H), 7.98-8.06 (m, 1H), 8.26 (d, 2H); MS: m/z 444.1 (MH⁺).

Compound 568 N-(5,5,5-Trifluoro-pentyl)-N-(3-isopropyl-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.43 (d, 3H), 1.53 (d, 3H), 1.53-1.78 (m, 4H), 1.94-2.19 (m, 2H), 3.14-3.30 (m, 1H), 3.62 (q, 1H), 3.80-4.00 (m, 1H), 7.31-7.42 (m, 2H), 7.64-7.73 (m, 1H), 7.92 (d, 2H), 7.98-8.08 (m, 1H), 8.26 (d, 2H); MS: m/z 500.1 (MH⁺).

Compound 675 N-(3-Cyclopropyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.59 (m, 4H), 1.38-1.63 (m, 1H), 4.24-5.37 (m, 2H), 7.36 (d, 3H), 7.54-7.67 (m, 2H), 7.70-7.90 (m, 4H), 8.04 (d, 2H); MS: m/z 550.0 (MH⁺).

Compound 698 N-(3-Cyclobutyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.59-2.44 (m, 6H), 3.67 (q, 1H), 4.44 (d, 1H), 5.26 (d, 1H), 7.26-7.54 (m, 3H), 7.54-7.67 (m, 2H), 7.80-7.93 (m, 1H), 7.95-8.11 (m, 3H), 8.19 (d, 2H), 13.64 (s, 1H); MS: m/z 562 (M-H)⁻.

Compound 755 N-(3-Cyclopropyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxyl-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.30-0.80 (m, 4H), 1.42-1.66 (m, 1H), 4.26-5.32 (m., 2H), 7.22-7.44 (m, 6H), 7.69-7.79 (m, 1H), 7.80-7.89 (m, 1H), 8.02 (d, 2H), 8.12-8.27 (m, 2H), 13.62 (s, 1H), MS: m/z 546.2 (M-H)⁻.

Compound 756 N-(3-Cyclobutyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.57-2.38 (m, 6H), 3.66 (t, 1H), 4.29 (d, 1H), 5.26 (d, 1H), 7.29-7.42 (m, 6H), 7.82-7.90 (m, 1H), 7.95-8.06 (m, 3H), 8.18 (d, 2H), 13.63 (s., 1H); MS: m/z 560.1 (M-H)⁻.

Compound 765 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-carboxy-propanesulfonamide

¹H-NMR (CDCl₃): δ 2.05 (s, 3H), 2.24 (q, 2H), 2.63 (t, 2H), 3.26-3.40 (m, 2H), 4.82 (s, 2H), 7.09 (t, 1H), 7.34-7.42 (m, 2H), 7.44-7.51 (m, 1H), 7.53-7.64 (m, 2H), 7.69-7.77 (m, 1H); MS: m/z 490.0 (MH⁺).

Compound 792 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-carboxy-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 2.00 (s, 3H), 4.54 (s, 2H), 4.90 (s, 2H), 7.32-7.52 (m, 3H), 7.57-7.75 (m, 3H), 7.86-7.96 (m, 1H), 13.64 (s, 1H); MS: m/z 462.0 (MH⁺).

Example 27

Compound 300-A was prepared from compound 1-C, following the procedure used to prepare compound 127-D.

N-(4-Fluoro-3-trifluorobenzyl)-N-(benzo[b]thiophen-2-yl)-[N′-tert-butyloxycarbonyl]-sulfonamide (300-B)

To a solution of chlorosulfonyl isocyanate (200 mg, 1.41 mmol) in CH₂Cl₂ (2 mL) was added tert-butanol (0.135 mL, 1.41 mmol) and the reaction was stirred at ambient temperature for 2 h. This solution was added drop-wise to a cooled (0° C.) solution of compound 300-A (485 mg; 1.34 mmol) in CH₂Cl₂ (2.5 mL) and pyridine (2.5 mL). The reaction mixture was stirred at ambient temperature for 18 h, diluted with EtOAc, washed with 1N HCl (2×), H₂O, brine, dried over Na₂SO₄, filtered, and the solvent was evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford compound 300-B as a yellow solid (0.389 g, 58%). ¹H-NMR (DMSO-d₆): δ 1.48 (s, 9H), 5.13 (s, 2H), 7.30 (s, 1H), 7.34-7.37 (m, 2H), 7.47-7.52 (m, 1H), 7.70-7.79 (m, 3H), 7.88-7.91 (m, 1H), 11.77 (s, 1H).

Compound 300 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-sulfamide

To compound 300-B (167 mg, 0.331 mmol) was added solution of 1N HCl in dioxane (6 mL) and the reaction was stirred at ambient temperature for 18 h. The reaction mixture was evaporated under reduced pressure, the residue dried under vacuo, and purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford compound 300 as a pink oil (0.097 g, 73%). ¹H-NMR (DMSO-d₆): δ 4.88 (s, 2H), 7.22 (s, 1H), 7.28-7.33 (m, 2H), 7.44-7.49 (m, 1H), 7.69-7.83 (m, 6H); MS: m/z 405.0 (MH⁺).

Example 28

N-(4-Fluoro-3-trifluorobenzyl)-N-(3-bromo-benzo[b]thiophen-2-yl)-[N′-tert-butyloxycarbonyl]-sulfonamide (301-A)

To a solution compound 300-B (306 mg; 0.606 mmol) in DCE (3 mL) was added N-bromosuccinimide (119 mg, 0.666 mmol) and the reaction was allowed to stir at ambient temperature for 2 h. The resultant solution was evaporated under reduced pressure and the crude residue purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford compound 301-A as a beige solid (0.254 mg, 72%). ¹H-NMR (DMSO-d₆): δ 1.51 (s, 9H), 5.06 (s, 1H), 7.41-7.46 (t, 1H), 7.49-7.54 (m, 2H), 7.62-7.66 (m, 1H), 7.70-7.77 (m, 2H), 8.00-8.03 (m, 1H), 11.81 (s, 1H).

Compound 301 N-(3-Bromo-benzo[b]thiophen-2-yl)-N (4-fluoro-3-trifluoromethyl-benzyl)-sulfamide

To compound 301-B (200 mg, 0.342 mmol) was added solution of 1N HCl in dioxane (6 mL) and the reaction was stirred at ambient temperature for 18 h. The reaction mixture was evaporated under reduced pressure, the residue dried under vacuo, and purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford compound 301 as a light purple oil (0.117 g, 71%). ¹H-NMR (DMSO-d₆): δ 3.16-3.17 (d, 2H), 4.80 (s, 2H), 7.39-7.49 (m, 3H), 7.67-7.82 (m, 3H), 7.96-7.98 (m, 1H); MS: m/z 483 (MH⁺).

Following the procedure described above for example 28 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 302 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-sulfamide

¹H-NMR (DMSO-d₆): δ 3.33 (s, 2H), 4.81 (s, 2H), 7.44-7.47 (t, 1H), 7.40-7.49 (m, 3H), 7.69-7.72 (m, 2H), 7.78-7.82 (m, 3H), 7.96-7.98 (m, 1H); MS: m/z 439.0 (MH⁺).

Example 29

Compound 757-A, was prepared by the method used to synthesize compound 1-C in Example 1, steps A and B. MS: m/z 164.1 (MH⁺).

N-(3-Methyl-benzo[b]thiophen-2-yl)-3-carbomethoxy-propanesulfonamide (757-B)

To a solution of compound 757-A (1.45 g, 7.25 mmol) and pyridine (1.42 mL, 17.6 mmol) in dichloromethane (20 mL), cooled to −10° C., was added 4-chlorosulfonyl-butyric acid methyl ester (1.6 g, 7.97 mmol) and the reaction mixture was stirred at ambient temperature for 2 days. The solvent was evaporated in vacuo, and the product was purified by flash column chromatography (SiO₂) eluting with an ethyl acetate (10-50%) in heptane gradient, to afford 1.75 g of compound 757-B as a pale orange solid. ¹H-NMR (DMSO-d₆): δ 1.87-2.10 (m, 2H), 2.32 (s, 3H), 2.42-2.58 (m, 2H), 3.11-3.29 (m, 2H), 3.59 (s, 3H), 7.25-7.48 (m, 2H), 7.71 (d, 1H), 7.77-7.94 (m, 1H), 10.07 (s, 1H); MS: m/z 328.0 (MH⁺).

Compound 757 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-carbomethoxy-propanesulfonamide

To a solution of compound 757-B (0.85 g, 2.59 mmol) in DMF (15 mL), cooled to 0° C., was added a solution of potassium t-butoxide (1.0 M in THF, 2.59 mL, 2.59 mmol) and the reaction mixture was stirred for 15 min. 4-Fluoro-3-trifluorobenzyl bromide (0.75 mL, 3.89 mL) was added in one-portion and the resultant solution was stirred at ambient temperature for 2 days. The reaction was partitioned between H₂O and EtOAc, the organic layer washed with water (3×), brine, dried over sodium sulfate, filtered, and the solvent was evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂), eluting with an ethyl acetate (5-40%) in heptane gradient, to afford 1.11 g of compound 757 as an oil. ¹H-NMR (CDCl₃): δ 2.04 (s, 3H), 2.24 (q, 2H), 2.45-2.62 (m, 2H), 3.23-3.43 (m, 2H), 3.71 (s, 3H), 4.82 (s, 2H), 7.09 (t, 1H), 7.32-7.43 (m, 2H), 7.43-7.52 (m, 1H), 7.52-7.65 (m, 2H), 7.73 (dd, 1H); MS: m/z 504.1 (MH⁺).

Following the procedure described above for example 29 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 310 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-chloro-pyridin-3-ylsulfonamide

MS: m/z 501.0 (MH⁺).

Compound 311 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-chloro-pyridin-5-ylsulfonamide

MS: m/z 501.0 (MH⁺).

Compound 315 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-N′,N′-dimethlysulfamide

MS: m/z 433.1 (MH⁺).

Compound 319 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-chloro-pyridin-3-ylsulfonamide

¹H-NMR (CDCl₃) δ 5.27 (s, 2H), 7.14 (t, 1H), 7.30 (dd, 1H), 7.38-7.46 (m, 2H), 7.57 (dd, 2H), 7.62-7.69 (m, 2H), 8.16 (dd, 1H), 8.59 (dd, 1H); MS: m/z 578.8 (MH⁺).

Compound 320 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-chloro-pyridin-5-ylsulfonamide

¹H-NMR (CDCl₃) δ 4.89 (s, 2H), 7.11 (t, 1H), 7.40-7.47 (m, 2H), 7.47-7.59 (m, 3H), 7.64-7.75 (m, 2H), 8.01 (dd, 1H), 8.83 (d, 1H); MS: m/z 580.9 (MH⁺).

Compound 321 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-chloro-pyridin-3-ylsulfonamide

MS: m/z 537.0 (MH⁺).

Compound 322 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3-fluoro-4-trifluoromethyl-benzyl)-pyridin-3-ylsulfonamide

¹H-NMR (CDCl₃) δ 4.95 (s, 2H), 7.18-7.25 (m, 2H), 7.39-7.49 (m, 2H), 7.49-7.61 (m, 2H), 7.63-7.75 (m, 2H), 8.11-8.19 (m, 1H), 8.91 (dd, 1H), 9.10 (d, 1H); MS: m/z 545.0 (MH⁺).

Compound 323 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-pyridin-3-ylsulfonamide

¹H-NMR (CDCl₃) δ 4.86 (s, 2H), 6.97-7.11 (m, 2H), 7.19 (dd, 1H), 7.39-7.48 (m, 2H), 7.58 (dd, 1H), 7.64-7.76 (m, 2H), 8.17 (dt, 1H), 8.90 (dd, 1H), 9.10 (d, 1H); MS: m/z 543.0 (MH⁺).

Compound 324 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-fluoro-5-chloro-benzyl)-pyridin-3-ylsulfonamide

¹H-NMR (CDCl₃) δ 4.96 (s, 2H), 6.88 (t, 1H), 7.20 (m, 1H), 7.39-7.48 (m, 3H), 7.51 (dd, 1H), 7.66-7.77 (m, 2H), 8.14 (dt, 1H), 8.88 (dd, 1H), 9.09 (d, 1H); MS: m/z 512.8 (MH⁺).

Compound 326 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-5-(2-methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-thien-2-ylsulfonamide

MS: m/z 633.9 (MH⁺).

Compound 327 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-5-carbomethoxy-furan-2-yl-sulfonamide

MS: m/z 527.8 (MH⁺).

Compound 328 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-1-methyl-3-trifluoromethyl-1H-pyrazol-4-ylsulfonamide

MS: m/z 551.8 (MH⁺).

Compound 329 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-5-(5-trifluoromethyl-isoxazol-3-yl)-thien-2-ylsulfonamide

MS: m/z 620.8 (MH⁺).

Compound 330 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-5-bromo-6-chloro-pyridin-3-ylsulfonamide

MS: m/z 594.8 (MH⁺).

Compound 331 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-5,6-dichloro-pyridin-3-ylsulfonamide

MS: m/z 550.8 (MH⁺).

Compound 332 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-pyrazol-1-yl-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.04-2.12 (m, 4H), 3.51 (br s, 1H), 6.53-6.63 (m, 1H), 7.06 (t, 1H), 7.30-7.40 (m, 2H), 7.40-7.49 (m, 1H), 7.55 (dd, 1H), 7.58-7.70 (m, 2H), 7.83 (d, 1H), 7.86-7.94 (m, 4H), 8.04 (d, 1H); MS: m/z 633.9 (MH⁺).

Compound 333 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-(5-methyl-[1,3,4]oxadiazol-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.07 (s, 3H), 2.63 (s, 3H), 3.50 (s, 2H), 7.07 (t, 1H), 7.32-7.40 (m, 2H), 7.40-7.49 (m, 1H), 7.50-7.57 (m, 1H), 7.58-7.67 (m, 2H), 7.70 (t, 1H), 7.90-7.99 (m, 2H), 8.38 (dt, 1H), 8.41-8.44 (m, 1H); MS: m/z 561.9 (MH⁺).

Compound 334 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-oxazol-5-yl-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.07 (s, 3H), 2.74 (br s, 2H), 7.06 (t, 1H), 7.29-7.41 (m, 2H), 7.41-7.48 (m, 1H), 7.48-7.70 (m, 4H), 7.77-7.86 (m, 2H), 7.86-7.93 (m, 2H), 8.08 (s, 1H); MS: m/z 546.9 (MH⁺).

Compound 336 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-(3-chloro-4-acetamide)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.07 (s, 3H), 2.32 (s, 3H), 3.52 (br s, 2H), 7.06 (t, 1H), 7.32-7.39 (m, 2H), 7.42 (d, 1H), 7.53 (dd, 1H), 7.58-7.63 (m, 1H), 7.64-7.69 (m, 1H), 7.72 (dd, 1H), 7.79-7.88 (m, 2H), 8.68 (d, 1H); MS: m/z 570.9 (MH⁺).

Compound 337 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-(6-chloro-imidazo[2,1-b]thiazol-5-yl-sulfonamide

¹H-NMR (CDCl₃): δ 2.06 (s, 3H), 3.53 (br s, 2H), 6.76 (d, 1H), 7.08 (t, 1H), 7.23 (d, 1H), 7.31-7.39 (m, 2H), 7.43-7.50 (m, 1H), 7.55-7.62 (m, 3H); MS: m/z 559.8 (MH⁺).

Compound 338 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-chloro-pyridin-3-ylsulfonamide

¹H-NMR (CDCl₃) δ 4.87 (s, 2H), 7.07-7.19 (m, 1H), 7.26 (s, 1H), 7.38-7.63 (m, 4H), 7.63-7.83 (m, 2H), 8.01 (dd, 1H), 8.83 (d, 1H); MS: m/z 536.8 (MH⁺).

Compound 367 N-(3,4-Difluoro-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 2.10 (s, 3H), 3.29 (s, 3H), 4.77 (s, 2H), 7.12-7.17 (m, 1H), 7.31-7.44 (m, 4H), 7.67-7.73 (m, 1H), 7.87-7.92 (m, 1H); MS: m/z 368.0 (MH⁺).

Compound 368 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 2.08 (s, 3H), 3.31 (s, 3H), 4.88 (s, 2H), 7.37-7.49 (m, 3H), 7.65-7.73 (m, 3H), 7.87-7.91 (m, 1H); MS: m/z 417.9 (MH⁺).

Compound 369 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-methanesulfonamide

¹H-NMR (DMSO-d₆): δ 2.04 (s, 3H), 3.29 (s, 3H), 4.81 (s, 2H), 7.29 (d, 2H), 7.35-7.42 (m, 4H), 7.65-7.71 (m, 1H), 7.87-7.92 (m, 1H); MS: m/z 416.0 (MH⁺).

Compound 379 N-(Benzo[b]thiophen-2-yl)-N-(3-carbomethoxy-benzyl)-pyridin-3-ylsulfonamide

MS: m/z 438.9 (MH⁺).

Compound 380 N-(Benzo[b]thiophen-2-yl)-N-(4-carbomethoxy-benzyl)-pyridin-3-ylsulfonamide

MS: m/z 438.9 (MH⁺).

Compound 383 N-(Benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-pyridin-3-ylsulfonamide

MS: m/z 401.1 (MH⁺).

Compound 384 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-2-oxo-2,3-dihydro-benzooxazol-6-yl-sulfonamide

¹H-NMR (DMSO-d₆) δ 1.64 (d, 3H), 2.21-2.31 (m, 3H), 2.38 (m, 3H), 7.30 (d, 1H), 7.39-7.51 (m, 2H), 7.55 (dd, 1H), 7.71 (d, 1H), 7.80 (dd, 1H), 7.84-7.93 (m, 1H), 7.95 (s, 1H), 12.3 (s, 1H); MS: m/z 470.9 (MH⁺).

Compound 405 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3-carbomethoxy-benzyl)-pyridin-3-ylsulfonamide

MS: m/z 518.8 (MH⁺).

Compound 406 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-carbomethoxy-benzyl)-pyridin-3-ylsulfonamide

MS: m/z 518.8 (MH⁺).

Compound 407 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-pyridin-3-yl-sulfonamide

MS: m/z 480.8 (MH⁺).

Compound 408 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-3-pyridin-3-yl-sulfonamide

MS: m/z 434.9 (MH⁺).

Compound 546 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-cyano-benzenesulfonamide

MS: m/z 505.0 (MH⁺).

Compound 547 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-isopropyl-benzo[b]thiophen-2-371)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.78 (d, 3H), 1.41 (d, 3H), 3.30 (q, 1H), 4.14 (d, 1H), 5.20 (d, 1H), 7.04 (t, 1H), 7.27-7.34 (m, 2H), 7.37-7.45 (m, 1H), 7.52-7.60 (m, 3H), 7.62-7.72 (m, 2H), 7.84-7.91 (m, 3H); MS: m/z 508.0 (MH⁺).

Compound 669 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2,2,2-trifluoro-ethanesulfonamide

MS: m/z 486.0 (MH⁺).

Compound 697 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2,2,2-trifluoro-ethane sulfonamide

MS: m/z 472.0 (MH⁺).

Compound 700 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-(2,2,2-trifluoro-acetyl)-1,2,3,4-tetrahydro-isoquinoline sulfonamide

MS: m/z 631.1 (MH⁺).

Compound 760 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3-trifluoromethoxy-benzyl)-2-carbomethoxy-ethane sulfonamide

MS: m/z 488.1 (MH⁺).

Example 30

N-(3-Methyl-benzo[b]thiophen-2-yl)-2-carbomethoxy-ethanesulfonamide (600-A)

A solution of compound 757-A (1.0 g, 5.01 mmol) and pyridine (851 μL, 10.5 mmol) in dichloromethane (20 mL), cooled to 10° C. was treated with 3-chlorosulfonyl-propionic acid methyl ester (716 μL, 5.25 mmol) and stirred at ambient temperature for 18 h. The solvent was evaporated in vacuo, and the crude residue purified by flash column chromatography (SiO₂), eluting with an ethyl acetate (10-50%) in heptane gradient to afford 1.1 g of compound 600-A as an off white solid. ¹H-NMR (DMSO-d₆): δ 2.31 (s, 3H), 2.82 (t, 2H), 3.43 (t, 2H), 3.62 (s, 3H), 7.24-7.50 (m, 2H), 7.58-7.77 (m, 1H), 7.80-7.95 (m, 1H), 10.17 (s, 1H); MS: m/z 314.1 (MH⁺).

Compound 600 N-(2-Cyclopropyl-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2-carbomethoxy-ethanesulfonamide

A solution of triphenylphosphine (0.251 g, 0.957 mmol) in THF (3 mL) was treated with DEAD (40% in toluene, 425 μL, 0.957 mmol) and stirred at ambient temperature for 5 min. Compound 600-A (0.20 g, 0.638 mmol) was added to the solution and stirred for 5 min. 2-Cyclopropyethanol (77 mL, 0.830 mmol) was added to the solution and the reaction mixture was stirred at ambient temperature for 18 h. The solvent was evaporated in vacuo, and the crude residue purified by flash column chromatography (SiO₂), eluting with an ethyl acetate (10-40%) in heptane gradient to afford 223 mg of compound 600 as a colorless oil. ¹H-NMR (CDCl₃): δ −0.02-0.06 (m, 2H), 0.35-0.52 (m, 2H), 0.56-0.80 (m, 1H), 1.49 (q, 2H), 2.40 (s, 3H), 2.81-2.97 (m, 2H), 3.41-3.57 (m, 2H), 3.64-3.84 (s superimposed on m, 5H), 7.33-7.49 (m, 2H), 7.59-7.80 (m, 2H); MS: m/z 382.4 (MH⁺).

Following the procedure described above for example 30 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 308 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-acetyl-benzenesulfonamide

MS: m/z 508.0 (MH⁺).

Compound 351 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-acetyl-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.52-1.73 (m, 2H), 2.24 (s, 3H), 2.29-2.46 (m, 2H), 2.67 (s, 3H), 3.49-3.67 (m, 2H), 7.36-7.48 (m, 2H), 7.76-7.94 (m, 5H), 8.16-8.19 (m, 2H); MS: m/z 456.0 (MH⁺).

Compound 352 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-acetyl-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.95 (s, 3H), 3.33 (s, 3H), 4.88 (s, 2H), 7.25-7.49 (m, 3H), 7.62-7.71 (m, 3H), 7.81-7.87 (m, 1H), 8.01-8.04 (d, 2H), 8.19-8.22 (d, 2H); MS: m/z 522.0 (MH⁺).

Compound 353 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-(2-methyl-pyrimidin-4-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.97 (s, 3H), 2.66 (s, 3H), 4.91 (s, 2H), 7.36-7.48 (m, 3H), 7.66-7.76 (m, 3H), 7.80-7.89 (m, 2H), 8.02-8.04 (d, 2H), 8.57-8.62 (m, 2H), 8.82-8.84 (d, 1H); MS: m/z 572.0 (MH⁺).

Compound 354 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-3-(2-methyl-pyrimidin-4-yl)-benzenesulfonamide

MS: m/z 506.0 (MH⁺).

Compound 355 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-8-methoxy-quinolin-5-ylsulfamide

¹H-NMR (DMSO-d₆): δ 1.76 (s, 3H), 4.07 (s, 3H), 4.91 (s, 2H), 7.19-7.45 (m, 4H), 7.52-7.63 (m, 4H), 7.59-7.81 (m, 1H), 8.23-8.26 (d, 2H), 8.81-8.84 (dd, 1H), 8.96-8.98 (m, 1H); MS: m/z 561.0 (MH⁺).

Compound 356 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-8-methoxyquinolin-5-ylsulfonamide

MS: m/z 495.0 (MH⁺).

Compound 370 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-cyano-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 5.05 (s, 2H), 7.22 (s, 1H), 7.31-7.37 (m, 2H), 7.46-7.52 (m, 4H), 7.69-7.74 (m, 3H), 7.82-7.92 (m, 2H), 8.04-8.07 (m, 1H), 8.26-8.29 (m, 1H), 8.43-8.44 (m, 1H).

Compound 372 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-(pyridin-4-yloxy)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.53-1.73 (m, 2H), 2.26 (s, 3H), 2.33-2.46 (m, 2H), 4.08 (m, 2H), 7.35-7.37 (m, 2H), 7.40-7.48 (m, 2H), 7.50-7.54 (m, 2H), 7.79-7.82 (m, 1H), 7.84-7.94 (m, 3H), 8.73-8.75 (d, 2H); MS: m/z 507.0 (MH⁺).

Compound 373 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-(pyridin-3-yloxy)-benzenesulfonamide

MS: m/z 507.0 (MH⁺).

Compound 411 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-cyano-benzenesulfonamide

MS: m/z 490.9 (MH⁺).

Compound 548 N-(2-Cyclopropyl-ethyl)-N-(3-isopropyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ −0.11-0.07 (m, 2H), 0.38-0.44 (m, 2H), 0.65 (m, 1H), 1.06-1.26 (m, 1H), 1.41 (d, 3H), 1.50 (d, 3H), 1.55-1.68 (m, 1H), 3.12-3.32 (m, 1H), 3.54-3.74 (m, 1H), 3.85-4.07 (m, 1H), 7.28-7.38 (m, 2H), 7.48-7.56 (m, 2H), 7.60-7.69 (m, 2H), 7.83 (d, 2H), 8.00 (dd, 1H); MS: m/z 400.0 (MH⁺).

Compound 549 N-(2-Cyclopropyl-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-cyano-benzenesulfonamide

¹H-NMR (CDCl₃): δ −0.07-0.08 (m, 2H), 0.44 (d, 2H), 0.54-0.77 (m, 1H), 1.32-1.52 (m, 2H), 2.38 (s, 3H), 3.37-3.87 (m, 2H), 7.40 (ddd, 2H), 7.59-7.78 (m, 3H), 7.91 (d, 1H), 7.99 (d, 1H), 8.10 (s, 1H); MS: m/z 397.0 (MH⁺).

Compound 550 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-3-cyano-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.27-2.65 (m, 2H) superimposed on 2.38 (s, 3H), 3.61-4.03 (m, 2H), 7.36-7.51 (m, 2H), 7.62-7.80 (m, 3H), 7.94 (d, 1H), 8.00 (d, 1H), 8.08 (s, 1H); MS: m/z 425.1 (MH⁺).

Compound 551 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-3-cyano-benzenesulfonamide

MS: m/z 439.0 (MH⁺).

Compound 552 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-3-cyano-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.52-1.74 (m, 4H), 1.93-2.20 (m, 2H), 2.39 (s, 3H), 3.23-3.91 (m, 2H), 7.33-7.50 (m, 2H), 7.60-7.79 (m, 3H), 7.91 (d, 1H), 7.97 (d, 1H), 8.07 (s, 1H); MS: m/z 453.0 (MH⁺).

Compound 573 N-(Benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-3-cyano-benzenesulfonamide

MS: m/z 410.7 (MH⁺).

Compound 574 N-(Benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-3-cyano-benzenesulfonamide

MS: m/z 424.6 (MH⁺).

Compound 575 N-(Benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-3-cyano-benzenesulfonamide

MS: m/z 382.8 (MH⁺).

Compound 601 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-2-carbomethoxy-ethanesulfonamide

¹H-NMR (CDCl₃): δ 2.36-2.57 ((m, 2H) superimposed on 2.42 (s, 3H), 2.81-2.96 (m, 2H), 3.42-3.59 (m, 2H), 3.75 (s, 3H), 3.81-4.00 (m, 2H), 7.43 (q, 2H), 7.68-7.82 (m, 2H); MS: m/z 382.4 (MH⁺).

Compound 602 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-2-carbomethoxy-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.73-1.90 (m, 2H), 2.10-2.33 (m, 2H), 2.42 (s, 3H), 2.77-2.94 (m, 2H), 3.37-3.57 (m, 2H), 3.65-3.84 (s superimposed on m, 5H), 7.32-7.50 (m, 2H), 7.62-7.84 (m, 2H); MS: m/z 424.2 (MH⁺).

Compound 603 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-2-carbomethoxy-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.65 (m, 4H), 1.94-2.20 (m, 2H), 2.41 (s, 3H), 2.76-2.99 (m, 2H), 3.36-3.56 (m, 2H), 3.69 (br s, 2H), 3.74 (s, 3H), 7.32-7.50 (m, 2H), 7.63-7.82 (m, 2H); MS: m/z 438.3 (MH⁺).

Compound 614 N-(2-Cyclopropyl-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ −0.12-0.06 (m, 2H), 0.31-0.47 (m, 2H), 0.53-0.73 (m, 1H), 1.30-1.51 (m, 2H), 2.36 (s, 3H), 3.35-3.86 (m, 2H), 7.30-7.43 (m, 2H), 7.47-7.55 (m, 2H), 7.59-7.72 (m, 3H), 7.79 (d, 2H); MS: m/z 372.1 (MH⁺).

Compound 615 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.34 (s, 3H), 2.35-2.50 (m, 2H), 3.53-4.03 (m, 2H), 7.35-7.46 (m, 2H), 7.49-7.57 (m, 2H), 7.62-7.75 (m, 3H), 7.77 (d, 1H), 7.80 (s, 1H); MS: m/z 400.0 (MH⁺).

Compound 616 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.70-1.84 (m, 2H), 2.14-2.35 (m, 2H), 2.36 (s, 3H), 3.40-3.78 (m, 2H), 7.32-7.45 (m, 2H), 7.47-7.56 (m, 2H), 7.60-7.74 (m, 3H), 7.77 (d, 2H); MS: m/z 414.0 (MH⁺).

Compound 617 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.51-1.74 (m, 4H), 1.93-2.18 (m, 2H), 2.36 (s, 3H), 3.41-3.69 (m., 2H), 7.32-7.44 (m, 2H), 7.47-7.55 (m, 2H), 7.60-7.73 (m, 3H), 7.74-7.80 (m, 2H); MS: m/z 428.1 (MH⁺).

Compound 670 N-(2-Cyclopropyl-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2,2,2-trifluoro-ethanesulfonamide

MS: m/z 378.0 (MH⁺).

Compound 671 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-2,2,2-trifluoro-ethanesulfonamide

MS: m/z 406.0 (MH⁺).

Compound 672 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-2,2,2-trifluoro-ethanesulfonamide

MS: m/z 420.0 (MH⁺).

Compound 673 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-2,2,2-trifluoro-ethanesulfonamide

MS: m/z 434.1 (MH⁺).

Compound 721 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-quinoxalin-5-yl-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.60-1.65 (m, 2H), 2.17 (s, 3H), 2.22-2.33 (m, 2H), 3.96-4.07 (m, 2H), 7.31-7.39 (m, 2H), 7.69-7.72 (m, 2H), 7.88-7.92 (m, 1H), 8.26-8.28 (m, 1H), 8.42-8.44 (m, 1H), 9.20-9.25 (m, 2H); MS: m/z 480.0 (MH⁺).

Compound 723 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-quinoxalin-5-yl-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.75 (s, 3H), 5.31 (s, 2H), 7.28-7.34 (m, 2H), 7.46-7.51 (m, 1H), 7.58-7.61 (m, 1H), 7.66-7.71 (m, 3H), 7.91-7.95 (m, 1H), 8.31-8.33 (m, 1H), 8.47-8.49 (m, 1H), 9.26-9.32 (m, 2H); MS: m/z 532.0 (MH⁺).

Compound 761 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-carbomethoxy-methanesulfonamide

MS: m/z 474.0 (MH⁺).

Compound 791 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-carbomethoxy-methanesulfonamide

¹H-NMR (CDCl₃): δ 1.96 (s, 3H), 3.91 (s, 3H), 4.25 (s, 2H), 4.95 (br s, 2H), 7.08 (t, 1H), 7.33-7.49 (m, 3H), 7.49-7.66 (m, 2H), 7.71-7.85 (m, 1H); MS: m/z 476.1 (MH⁺).

Compound 794 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-2-carbomethoxy-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.96 (s, 3H), 2.85-2.97 (m, 2H), 3.48-3.61 (m, 2H), 3.75 (s, 3H), 4.78 (br s, 2H), 7.11 (d, 2H), 7.28-7.42 (m, 4H), 7.55-7.62 (m, 1H), 7.70-7.77 (m, 1H); MS: m/z 488.1 (MH⁺).

Example 31

Compound 346 N-(3-Dimethylaminomethyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-ethanesulfonamide

To a solution of compound 210 (0.116 g, 0.26 mmol) in dichloromethane (4 mL) was added dimethylamine (2 M in THF, 195 μL, 0.39 mmol) and the reaction mixture stirred at ambient temperature for 15 min. Sodium triacetoxyborohydride (0.11 g, 0.52 mmol) was added to the reaction mixture and stirred at ambient temperature for 6 h. The solution was treated with saturated aqueous sodium bicarbonate, the organic layer separated, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by reverse phase prep HPLC (eluting with an 20-90% acetonitrile in water with 0.1% TFA gradient) to afford the 90 mg of compound 346 as the TFA salt (90 mg, 59%)

MS: m/z 475.2 (MH⁺).

Following the procedure described above for example 31 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 347 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methylaminomethyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

MS: m/z 461.2 (MH⁺).

Compound 348 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-propylaminomethyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

MS: m/z 489.3 (MH⁺).

Compound 349 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-pyrrolidin-1-yl-methyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

MS: m/z 501.2 (MH⁺).

Compound 381 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-pyrrolidin-1-yl-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

MS: m/z 549.3 (MH⁺).

Compound 417 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methylaminomethyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

MS: m/z 509.1 (MH⁺).

Compound 418 N-(3-Dimethylaminomethyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

MS: m/z 523.2 (MH⁺).

Compound 420 N-(3-Dimethylaminomethyl-benzo[b]thiophen-2-yl)-N-(butyl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 461.27 (MH⁺).

Example 32

3-Cyclopropyl-benzo[b]thiophene-2-carboxylic acid ethyl ester (674-B)

To a suspension of 60% NaH (0.26 g; 7.74 mmol) in THF (10 mL), at ambient temperature, was added ethyl thioglycolate (0.86 g; 7.14 mmol) drop-wise, and the reaction was stirred at ambient temperature for 30 min. Compound 674-A (0.98 g; 5.96 mmol) was added in one-portion. The reaction was allowed to reflux for 18 h, cooled, diluted with EtOAc, washed sequentially with 1N NaOH, H₂O, and brine, dried over Na₂SO₄, filtered, and the filtrate was concentrated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂), eluting with a heptane-EtOAc gradient to afford 0.484 g of compound 674-B as an oil. ¹H-NMR (DMSO-d₆): δ 1.08-1.16 (m, 4H), 1.32-1.36 (t, 3H), 2.36-2.51 (m, 1H), 4.31-4.37 (q, 2H), 7.32-7.54 (m, 2H), 7.64-7.75 (m, 1H), 7.99-8.05 (m, 1H); MS: m/z 247.1 (MH⁺).

3-Cyclopropyl-benzo[b]thiophene-2-carboxylic acid (674-C)

A solution of compound 674-B (2.68 g, 10.9 mmol) in ethanol (30 mL) was treated with 3N aqueous sodium hydroxide (5.4 mL, 16.2 mmol) and refluxed for 2 h. The solution was cooled, and the solvent was evaporated in vacuo. The residue was dissolved in water and washed with dichloromethane. The aqueous phase was acidified with concentrated hydrochloric acid, and the product was extracted into ethyl acetate, washed with brine, dried over Na₂SO₄, filtered and the solvent was evaporated in vacuo, to afford 1.9 g of compound 674-C as a colorless solid. ¹H-NMR (DMSO-d₆): δ 0.58-1.37 (m, 4H), 2.44-2.47 (m, 1H), 7.13-7.61 (m, 2H), 7.98 (dd, 2H), 13.33 (br s, 1H).

2-Amino-3-cyclopropyl-benzo[b]thiophene (674-D)

A solution of compound 647-C (6.9 g, 31.6 mmol) and diisopropylethylamine (6.63 mL, 37.9 mmol) in t-butanol (100 mL) was treated with DPPA (8.2 mL, 37.9 mmol) and refluxed for 4 h. The solvent was evaporated in vacuo, and the crude residue was purified by flash column chromatography (SiO₂) eluting an ethyl acetate (0-15%) in heptane gradient, to afford 7.1 g of the BOC-protected amine (MS: m/z 290.1 (MH⁺)). The BOC-protected amine was dissolved in a solution of 4N HCl in dioxane (100 mL) and stirred at ambient temperature for 4 h. The solid precipitate was collected by filtration, washed with diethyl ether and dried under vacuo to afford 2.36 g of the hydrochloride salt of compound 674-D as a colorless solid. The combined solvents were evaporated in vacuo to afford 3.1 g of additional 674-D as a yellow solid. MS: m/z 190.1 (MH⁺).

N-(3-Cyclopropyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide (674-E)

A solution of compound 674-D (0.60 g, 2.07 mmol) and pyridine (343 μL, 4.25 mmol) in dichloromethane, cooled to −10° C. was treated with 4-chlorosulfonylbenzoic acid (0.480 g, 2.17 mmol) and stirred at ambient temperature for 2 days. The solution was cooled to −10° C. and treated with additional portions of pyridine (120 μL) and 4-chlorosulfonylbenzoic acid (0.16 g) and stirred at ambient temperature for 18 h. The reaction mixture was partitioned between 2N HCl and ethyl acetate, the organic layer washed with brine, dried over sodium sulfate, filtered, and the solvent evaporated under reduced pressure to afford 0.95 g of the crude acid. The crude acid was suspended in methanol (25 mL), treated with sulfuric acid (0.1 mL) and refluxed for 6 h. The yellow solid was filtered, the solution concentrated in vacuo, diluted with water, extracted with ethyl acetate, the organic layer washed with brine, dried over sodium sulfate, filtered and the solvent evaporated under reduced pressure. The crude material was purified by flash column chromatography (SiO₂), eluting with an ethyl acetate (10-50%) gradient to afford 0.483 g of compound 674-E as a yellow oil. MS: m/z 388.0 (MH⁺).

Compound 674 N-(3-Cyclopropyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide

To a solution of compound 674-E (0.176 g, 0.454 mmol) in DMF (3 mL), cooled to 0° C. was added a solution of potassium t-butoxide (1.0 M in THF, 454 μL, 0.454 mmol) and the reaction mixture was stirred for 15 min. 4-Fluoro-3-trifluorobenzyl bromide (131 μL, 0.681 mmol) was added and the solution was stirred at ambient temperature for 18 h. The solution was diluted with water (20 mL), extracted with ethyl acetate, and the organic layer was washed with brine, dried over sodium sulfate, filtered, and the solvent evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an ethyl acetate-heptane (10-50%) gradient to afford 0.187 g of compound 674 as an oil. ¹H-NMR (CDCl₃): δ 0.65-0.99 (m, 4H), 1.42-1.67 (m, 1H), 3.99 (s, 3H), 4.16-5.33 (m, 2H), 7.05 (t, 1H), 7.30-7.46 (m, 3H), 7.55 (dd, 1H), 7.59-7.70 (m, 1H), 7.70-7.84 (m, 1H), 7.92 (d, 2H), 8.20 (d, 2H); MS: m/z 564.2 (MH⁺).

Following the procedure described above for example 32 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 325 N-(3-Trifluoromethyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-benzenesulfonamide

Compound 325 was prepared substituting 2-fluoro-2,2,2,-trifluoroacetopheneone for cyclopropyl-(2-fluoro-phenyl)-methanone, triethylamine for NaH and acetonitrile for THF in Step A of Example 32. ¹H-NMR (CDCl₃): δ 4.57 (br s, 1H), 4.89 (br s, 1H), 7.08 (d, 2H), 7.18-7.35 (m, 2H), 7.37-7.49 (m, 2H), 7.49-7.62 (m, 2H), 7.62-7.75 (m, 2H), 7.83 (d, 3H); MS: m/z 531.9 (MH⁺).

Compound 501 N-(3-Cyclopentyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 564.2 (MH⁺).

Compound 696 N-(3-Cyclobutyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoro methyl-benzyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.91 (m, 3H), 2.17-2.60 (m, 3H), 3.66-3.89 (m, 1H), 3.99 (s, 3H), 4.11-4.34 (m, 1H), 5.07-5.27 (m, 1H), 6.99-7.15 (m, 1H), 7.37 (dd, 3H), 7.49-7.59 (m, 1H), 7.61-7.71 (m, 1H), 7.88 (d, 2H), 7.99-8.10 (m, 1H), 8.19 (d, 2H); MS: m/z 578.1 (MH⁺).

Compound 753 N-(3-Cyclopropyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.44-0.79 (m, 4H), 1.22-1.63 (m, 1H), 3.99 (s, 3H), 4.30-5.15 (m, 2H), 7.08 (d, 2H), 7.25-7.37 (m, 4H), 7.60-7.68 (m, 1H), 7.74-7.83 (m, 1H), 7.91 (d, 2H), 8.15-8.25 (m, 2H); MS: m/z 562.0 (MH⁺).

Compound 754 N-(3-Cyclobutyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.59-2.11 (m, 4H), 2.13-2.49 (m, 3H), 3.99 (s, 3H), 4.16 (d, 1H), 5.17 (d, 1H), 7.09 (d, 2H), 7.23-7.43 (m, 4H), 7.60-7.71 (m, 1H), 7.89 (d, 2H), 7.97-8.07 (m, 1H), 8.14-8.26 (m, 2H); MS: m/z 576.2 (MH⁺).

Example 33

1-Bromo-3-methyl-butan-2-one (563-B)

To a solution of compound 563-A (6.0 g; 69.7 mmol) dissolved in MeOH (40 mL) and cooled to 0° C., was added bromine (3.56 mL; 69.7 mmol), at a rate such that the internal temperature did not exceed 10° C. The reaction was allowed to stir for 45 min at 5-10° C., to which was then added H₂O (20 mL) and the reaction was stirred for an additional 18 h at ambient temperature. Water was added to the reaction mixture, which was then extracted with diethyl ether. The combined ether extracts were washed sequentially with 10% aq. NaHCO₃, H₂O, and brine, dried over Na₂SO₄, filtered, and the filtrate was evaporated under reduced pressure to afford compound 563-B as an oil. ¹H-NMR (CDCl₃): δ 1.10-1.17 (d, 6H), 2.95-3.02 (m, 1H), 3.98 (s, 2H).

3-Methyl-1-phenylsulfanyl-butan-2-one (563-C)

To a solution of thiophenol (4.44 mL; 43.4 mmol) in diethyl ether (29 mL) was added pyridine (17.2 mL; 0.21 mol), followed by the drop-wise addition of a solution of compound 563-B (7.18 g; 43.5 mmol) in diethyl ether (15 mL), at ambient temperature, and the reaction was stirred for 72 h. The reaction was diluted with EtOAc, washed with 2N HCl, H₂O, brine, dried over Na₂SO₄, filtered and the solvent evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford compound 563-C as an oil. ¹H-NMR (CDCl₃): δ 1.09-1.10 (d, 6H), 2.90-2.97 (m, 1H), 3.75 (s, 2H), 7.18-7.35 (m, 5H).

3-Isopropyl-benzo[b]thiophene (563-D)

To a hot solution (136° C.) of PPA (8.2 g) in chlorobenzene (50 mL) is added a solution of compound 563-C (4.34 g; 22.4 mmol) in chlorobenzene (35 mL). The reaction was stirred at 136° C. for 18 h, cooled to ambient temperature, diluted with EtOAc, quenched with H₂O, and the EtOAc layer was washed with H₂O, brine, dried over Na₂SO₄, filtered and the solvent evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂), eluting with a heptane-EtOAc gradient to afford compound 563-D as an oil. ¹H-NMR (DMSO-d₆): δ 1.31-1.33 (d, 6H), 3.26-3.31 (m, 1H), 7.33-7.43 (m, 2H), 7.83-7.85 (m, 1H), 7.95-7.97 (m, 1H); MS: m/z 328.0 (MH⁺).

3-Isopropyl-benzo[b]thiophene-2-carboxaldehyde (563-E)

To a solution of compound 563-D (3.8 g, 21.5 mmol) in THF (70 mL), cooled to −70 to −78° C. was added a solution of n-butyl lithium (2.5 M in hexanes, 8.6 mL, 21.5 mmol), drop-wise. The reaction mixture was allowed to warm slowly to −20° C., then re-cooled to −73° C. DMF (2.5 mL) was added drop-wise to the solution at −70 to −78° C. The reaction mixture was allowed to warm ambient temperature and stirred for 18 h. The reaction mixture was cooled on an ice bath, and quenched with several ice chips. The reaction mixture was treated with saturated aqueous NH₄Cl, extracted with ethyl acetate, and the organic phase washed with brine, dried over Na₂SO₄, filtered, and the solvent was evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂), eluting with an ethyl acetate (0-10%) in heptane gradient, to afford 2.06 g of compound 563-E as a yellow oil. ¹H-NMR (CDCl₃): δ 1.60 (d, 6H), 3.99 (q, 1H), 7.33-7.61 (m, 2H), 7.87 (d, 1H), 8.05 (d, 1H), 10.44 (s, 1H); MS: m/z 205.1 (MH⁺).

3-Isopropyl-benzo[b]thiophene-2-carboxylic acid (563-F)

A solution of compound 563-E (1.95 g, 9.5 mmol) in acetone (30 mL) was refluxed for 30 min. A mixture of potassium permanganate (3.02 g, 19.1 mmol) in water (10 mL) was added in portions, and the resultant mixture was refluxed for an additional 30 min. The mixture was cooled to ambient temperature and concentrated in vacuo. A solution of aqueous Na₂SO₃ (1M, 50 mL) was added followed by sulfuric acid (1 M, 50 mL). Two additional portions of Na₂SO₃ (1M, 20 mL) were added followed by sulfuric acid (1 M, 20 mL), which resulted in the disappearance of the dark brown color. The resultant suspension was diluted with H₂O, filtered, washed with H₂O and dried under vacuo to afford 1.52 g of compound 563-F as a yellow solid. MS: m/z 221.1 (MH⁺).

2-Amino-3-isopropyl-benzo[b]thiophene, hydrochloride (563-G)

A solution of compound 563-F (1.52 g, 6.90 mmol) and DIEA (1.45 mL, 8.27 mmol) in t-butanol (30 mL) was treated with DPPA (1.8 mL, 8.27 mmol) and refluxed for 6 h. The reaction mixture was cooled and the solvent evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an ethyl acetate (0-20%) in heptane gradient, to afford 1.41 g of the BOC-protected amine (not shown). ¹H-NMR (CDCl₃): δ 1.41 (d, 6H), 1.55 (s, 9H), 3.26 (dt, 1H), 6.74 (br s, 1H), 7.12-7.39 (m, 2H), 7.57-7.86 (m, 2H); MS: m/z 292.2 (MH⁺). The BOC-protected amine (1.41 g, 4.84 mmol) was dissolved in 4N HCl in dioxane (20 mL) and stirred at ambient temperature for 6 h. The suspension was diluted with diethyl ether, the solid filtered, washed with diethyl ether, and dried under vacuo to afford 1.09 g of the hydrochloride salt of compound 563-G as a pale yellow solid. ¹H-NMR (DMSO-d₆): δ 1.35 (d, 6H), 3.33 (q, 1H), 7.03-7.20 (m, 1H), 7.27 (t, 1H), 7.73 (dd, 2H), 8.73 (br s, 1H); MS: m/z 192.0 (MH⁺).

N-(3-Isopropyl-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

A solution of compound 563-G (0.774 g, 3.40 mmol) and pyridine (577 μL, 7.14 mmol) in dichloromethane, cooled to −10° C., was treated with chlorosulfonyl-benzoic acid (0.787 g, 3.56 mmol) and the reaction mixture was stirred at ambient temperature for 4 h. The solvent was evaporated in vacuo, the residue treated with 2N HCl, the aqueous phase extracted with ethyl acetate, the organic phase washed with brine, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo to afford 1.16 g of the crude benzoic acid (not shown). ¹H-NMR (DMSO-d₆): δ 1.15 (d, 6H), 3.25 (dt, 1H), 7.25-7.37 (m, 2H), 7.67-7.99 (m, 4H), 8.13 (d, 2H), 10.66 (s, 1H); MS: m/z 192.0 (MH⁺).

N-(3-Isopropyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide (563-H)

A solution of the crude benzoic acid (1.1 g, 2.93 mmol) and sulfuric acid (0.15 mL) in methanol (30 mL) was refluxed for 13 h. The solution cooled, concentrated in vacuo, and partitioned between dichloromethane and water. The organic layer was separated, and by flash column chromatography (SiO₂) eluting with an ethyl acetate (5-40%) in heptane gradient to afford 0.9 g of compound 563-H as a pale pink solid. ¹H-NMR (DMSO-d₆): δ 1.16 (d, 6H), 3.26 (dt, 1H), 3.89 (s, 3H), 7.28-7.34 (m, 2H), 7.73-7.83 (m, 1H), 7.83-7.95 (m, 3H), 8.15 (d, 2H), 10.67 (s, 1H); MS: m/z 390.1 (MH⁺).

Compound 563 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-isopropyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

A solution of compound 563-H (0.30 g, 0.77 mmol) in DMF (6 mL), at 0° C., was treated with a solution of potassium t-butoxide (1.0 M in THF, 0.81 mL, 0.81 mmol) and stirred for 10 min. 4-Fluoro-3-trifluoromethylbenzyl bromide (293 μL, 1.54 mmol) was added and the resultant solution was stirred at ambient temperature for 18 h. Water was added, the reaction mixture extracted with ethyl acetate, and the organic layer was washed with water (3×), brine, dried over Na₂SO₄, filtered, and the solvent was evaporated in vacuo. The product was purified by flash column chromatography (SiO₂) eluting with an ethyl acetate (1-35%) in heptane gradient to afford 0.29 g of compound 563 as a colorless solid. ¹H-NMR (CDCl₃): δ 0.77 (d, 3H), 1.42 (d, 3H), 3.17-3.35 (m, 1H), 4.00 (s, 3H), 4.14 (d, 1H), 5.23 (d, 1H), 7.06 (t, 1H), 7.28-7.36 (m, 2H), 7.38-7.45 (m, 1H), 7.58 (dd, 1H), 7.65 (dd, 1H), 7.85-7.95 (m, 3H), 8.22 (d, 2H); MS: m/z 566.0 (MH⁺).

Example 34

N-(Butyl)-N-(benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

Compound 430-A was prepared utilizing Compound 1-C, Example 32, steps E and F, and Example 3, step A. MS: m/z 404.2 (MH⁺).

Compound 430 N-(Butyl)-N-(1,1-dioxo-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

A solution of compound 430-A (0.199 g, 0.493 mmol) in chloroform (10 mL) was treated with meta-chloroperbenzoic acid (77%, 0.243 g, 1.08 mmol), and the reaction mixture was stirred at ambient temperature for 18 h. The mixture was washed with saturated aqueous sodium bicarbonate, dried over sodium sulfate, filtered and the solvent evaporated in vacuo. The crude residue was purified flash column chromatography (SiO₂), eluting with an ethyl acetate (10-50%) in heptane gradient to afford 0.120 g of compound 430 as a colorless solid. ¹H-NMR CDCl₃): δ 0.94 (t, 3H), 1.35-1.48 (m, 2H), 1.71-1.82 (m, 2H), 3.81 (t, 2H), 3.93 (s, 3H), 7.24 (s, 1H), 7.36 (d, 1H), 7.44-7.50 (m, 1H), 7.54-7.90 (m, 2H), 7.94 (d, 2H), 8.14 (d, 2H); MS: m/z 436.2 (MH⁺).

Following the procedure described above for example 34 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 421 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(1,1-dioxo-benzo[b]thiophen-2-yl)-benzenesulfonamide

MS: m/z 498.1 (MH⁺).

Compound 431 N-(3-Bromo-1,1-dioxo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

The precursor, N-(3-bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide, was synthesized from N-(benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide as per Example 5, step A. ¹H-NMR (CDCl₃): δ 4.76 (br s, 2H), 7.08 (t, 1H), 7.51-7.72 (m, 8H), 7.76 (dd, 1H), 8.10 (d, 2H); MS: m/z 576 & 578.1 (MH⁺).

Compound 433 N-(3-Bromo-1,1-dioxo-benzo[b]thiophen-2-yl)-N-(butyl)-4-carbomethoxy-benzenesulfonamide

The precursor, N-(3-bromo-benzo[b]thiophen-2-yl)-N-(butyl)-4-carbomethoxy-benzenesulfonamide, was synthesized from N-(benzo[b]thiophen-2-yl)-N-(butyl)-4-carbomethoxy-benzenesulfonamide as per Example 5, step A. ¹H-NMR (CDCl₃): δ 0.89 (t, 3H), 1.36 (m, 2H), 1.69 (q, 2H), 3.53-3.65 (m, 2H), 3.97 (s, 3H), 7.60-7.76 (m, 4H), 8.12-8.18 (m, 2H), 8.19-8.25 (m, 2H); MS: m/z 514 & 516.0 (MH⁺).

Compound 460 N-(3-Acetyl-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

The precursor, N-(3-acetyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide, was synthesized from N-(benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carbomethoxy-benzenesulfonamide as per Example 14, step A. ¹H-NMR (CDCl₃): δ 2.27 (s, 3H), 4.96 (s, 2H), 7.19 (t, 1H), 7.48-7.74 (m, 7H), 7.79-7.89 (m, 1H), 7.89-8.00 (m, 3H); MS: m/z 540.2 (MH⁺), 562.0 (MNa⁺).

Compound 463 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-[3-(1-hydroxy-1-methyl-ethyl)-1,1-dioxo-benzo[b]thiophen-2-yl]-benzenesulfonamide

The precursor, N-(4-fluoro-3-trifluoromethyl-benzyl)-N-[3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl]-benzenesulfonamide, was synthesized from N-(3-acetyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide as per Example 19, step A. ¹H-NMR (CDCl₃): δ 1.46 (s, 3H), 1.78 (s, 3H), 3.52 (br s, 1H), 4.88 (d, 1H), 4.95 (d, 1H), 7.05 (t, 1H), 7.45-7.49 (m, 2H), 7.52-7.68 (m, 3H), 7.69-7.73 (m, 3H), 7.79 (dd, 1H), 7.92 (d, 2H); MS: m/z 538.0 (M-OH)⁺, 578.1 (MNa⁺).

Compound 464 N-(3,4-Difluoro-benzyl)-N-[3-(1-hydroxy-ethyl)-1,1-dioxo-benzo[b]thiophen-2-yl]-benzenesulfonamide

The precursor, N-(3,4-difluorobenzyl)-N-[3-(1-hydroxy-1-ethyl)-benzo[b]thiophen-2-yl]benzenesulfonamide, was synthesized from N-(3-acetyl-benzo[b]thiophen-2-yl)-N-(3,4-difluorobenzyl)-benzenesulfonamide as per Example 18, step A. ¹H-NMR (CDCl₃): δ 1.04 (d, 3H), 4.58 (d, 1H), 4.87-4.93 (m, 2H), 7.08-7.18 (m, 1H), 7.41-7.45 (m, 1H), 7.53-7.72 (m, 7H), 7.95 (d, 1H), 8.04 (d, 2H); MS: m/z 474.1 (M-OH)⁺, 514.0 (MNa⁺).

Compound 577 N-(3-Bromo-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-N-(2-cyclopropylethyl)-benzenesulfonamide

The precursor, N-(3-bromo-benzo[b]thiophen-2-yl)-N-(2-cyclopropylethyl)-benzenesulfonamide, was synthesized from N-(benzo[b]thiophen-2-yl)-N-(2-cyclopropylethyl)-benzenesulfonamide as per Example 5, step A. ¹H-NMR (CDCl₃): δ −0.02-0.06 (m, 2H), 0.24-0.47 (m, 2H), 0.52-0.75 (m, 1H), 1.47-1.73 (m, 2H), 3.48-3.80 (m, 2H), 7.49-7.79 (m, 7H), 8.03-8.19 (m, 2H); MS: m/z 468 & 470.1 (MH⁺).

Compound 618 N-(2-Cyclopropyl-ethyl)-N-(3-methyl-1,1-dioxo-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.02-0.09 (m, 2H), 0.27-0.49 (m, 2H), 0.51-0.74 (m, 1H), 1.45-1.75 (m, 2H), 2.38 (s, 3H), 3.66 (t, 2H), 7.42-7.71 (m, 7H), 7.97-8.30 (m, 2H); MS: m/z 404.1 (MH⁺).

Compound 619 N-(3-Methyl-1,1-dioxo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.39 (s, 3H), 2.44-2.70 (m, 2H), 3.86 (t, 2H), 7.47-7.62 (m, 4H), 7.62-7.72 (m, 3H), 8.05 (d, 2H); MS: m/z 432.0 (MH⁺).

Compound 620 N-(3-Methyl-1,1-dioxo-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.77-2.03 (m, 2H), 2.04-2.31 (m, 2H), 2.40 (s, 3H), 3.67 (t, 2H), 7.49-7.61 (m, 4H), 7.61-7.69 (m, 3H), 8.01-8.05 (m, 2H); MS: m/z 446.1 (MH⁺).

Compound 621 N-(3-Methyl-1,1-dioxo-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.36-1.68 (m, 2H), 1.70-1.84 (m, 2H), 1.91-2.20 (m, 2H), 2.39 (s, 3H), 3.60 (t, 2H), 7.47-7.60 (m, 4H), 7.60-7.69 (m, 3H), 8.01-8.07 (m, 2H); MS: m/z 460.0 (MH⁺).

Compound 622 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-1,1-dioxo-benzo[b]thiophen-2-yl)-benzenesulfonamide

MS: m/z 512.0 (MH⁺).

Compound 632 N-(2-Cyclopropyl-ethyl)-N-(3-methyl-1,1-dioxo-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

MS: m/z 447.7 (MH⁺).

Compound 633 N-(3-Methyl-1,1-dioxo-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-carboxy-benzenesulfonamide

MS: m/z 503.7 (MH⁺).

Compound 634 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-1,1-dioxo-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

MS: m/z 555.6 (MH⁺).

Example 35

Compounds 434, 435, 436 N-(Butyl)-N-(3-methoxy-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide, N-(butyl)-N-(3-bromo-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide, and N-(butyl)-N-(3-methoxy-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

A solution of compound 433 (0.525 g, 1.02 mmol) in methanol (10 mL) was treated with 1N sodium hydroxide (1.3 mL, 1.3 mmol) and refluxed for 30 minutes. The solution was cooled, neutralized with 1N hydrochloric acid the solvent evaporated in vacuo, and the crude residue purified by reverse phase pHPLC (C₁₈) using a gradient of acetonitrile (30-90%) in water (0.1% TFA), to afford 0.015 g of compound 434, 0.050 g of compound 435, and 0.15 g of compound 436.

Compound 434 N-(Butyl)-N-(3-methoxy-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.94 (t, 3H), 1.33-1.43 (m, 2H), 1.78-1.86 (m, 2H), 3.70 (t, 2H), 4.47 (s, 3H), 7.58-7.70 (m, 4H), 8.17 (d, 2H), 8.30 (d, 2H); MS: m/z 452.1 (MH⁺).

Compound 435 N-(Butyl)-N-(3-bromo-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.90 (t, 3H), 1.33-1.42 (m, 2H), 1.67-1.74 (m, 2H), 3.61 (t, 2H), 7.60-7.74 (m, 4H), 8.19 (d, 2H), 8.28 (d, 2H); MS: m/z 500 & 502.0 (MH⁺).

Compound 436 N-(Butyl)-N-(3-methoxy-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.93 (t, 3H), 1.32-1.41 (m, 2H), 1.74-1.82 (m, 2H), 3.65 (t, 2H), 3.96 (s, 3H), 4.44 (s, 3H), 7.55-7.70 (m, 4H), 8.10 (d, 2H), 8.18 (d, 2H); MS: m/z 466.2 (MH⁺).

Example 36

Compound 644 N-(2-Cyclopropylethyl)-N-(3-methylamino-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-benzenesulfonamide

A solution of compound 577 (56 mg, 0.120 mmol) in THF (1 mL) was treated with a solution of methylamine in THF (2.0 M, 1 mL, 2.0 mmol) and stirred at ambient temperature for 1 h. The solvent was evaporated in vacuo and the crude residue purified by reverse phase pHPLC, eluting with an acetonitrile (20-90%) in water (0.1% TFA) gradient to afford 30 mg of compound 644 as a colorless solid. ¹H-NMR (DMSO-d₆): δ −0.01-0.03 (m, 2H), 0.19-0.47 (m, 2H), 0.47-0.77 (m, 1H), 1.20-1.47 (m, 1H), 1.66 (tt, 1H), 3.19 (d, 3H), 3.47 (td, 1H), 3.65 (td, 1H), 7.32-7.89 (m, 7H), 7.84-8.14 (m, 3H); MS: m/z 419.1 (MH⁺).

Following the procedure described above for example 36 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 536 N-(Butyl)-N-(3-dimethylamino-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

MS: m/z 465.1 (MH⁺).

Compound 643 N-(2-Cyclopropylethyl)-N-(3-dimethylamino-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ −0.02-0.06 (m, 2H), 0.25-0.46 (m, 2H), 0.51-0.74 (m, 1H), 1.47-1.86 (m, 2H), 3.03-3.27 (s, 6H), 3.62 (td, 1H), 3.70-3.90 (m, 1H), 7.42-7.71 (m, 7H), 8.02 (d, 2H); MS: m/z 433.0 (MH⁺).

Compound 645 N-(2-Cyclopropyl-ethyl)-N-[3-(4-methyl-piperazin-1-yl)-1,1-dioxo-1H-1λ⁶-benzo[b]thiophen-2-yl]-benzenesulfonamide

MS: m/z 488.1 (MH⁺).

Compound 646 N-(3-Amino-1,1-dioxo-1H-benzo[b]thiophen-2-yl)-N-(2-cyclopropylethyl)-benzenesulfonamide

MS: m/z 405.1 (MH⁺).

Compound 647 N-(2-Cyclopropyl-ethyl)-N-(1,1-dioxo-3-piperazin-1-yl-1H-1λ⁶-benzo[b]thiophen-2-yl)-benzenesulfonamide

MS: m/z 474.1 (MH⁺).

Compound 648 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methylamino-1,1-dioxo-1H-1λ⁶-benzo[b]thiophen-2-yl)-benzenesulfonamide

MS: m/z 527.1 (MH⁺).

Compound 649 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-[3-(4-methyl-piperazin-1-yl)-1,1-dioxo-benzo[b]thiophen-2-yl]-benzenesulfonamide

MS: m/z 596.1 (MH⁺).

Example 37

N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-carboxy-benzo[b]thiophen-2-yl)-benzenesulfonamide (458-A)

A solution of compound 207 (0.4 g, 0.81 mmol) in acetone 1 (15 mL) was heated to reflux and treated with a solution of potassium permanganate (0.192 g, 1.21 mmol) in water (˜3 mL). The resultant mixture was refluxed for an additional 2 h. The mixture was concentrated in vacuo, diluted with water, treated with 1M Na₂SO₃ (4 mL) and 1M sulfuric acid (4 mL). The clear colorless solution was extracted with dichloromethane, washed with 1N hydrochloric acid, dried over sodium sulfate, filtered and the solvent was evaporated in vacuo to afford 0.41 g of compound 458-A as a colorless solid. ¹H-NMR (CDCl₃): δ 4.88 (s, 2H), 7.04 (t, 1H), 7.30-7.79 (m, 10H), 8.32 (d, 1H); MS: m/z 510.0 (MH⁺).

Compound 458 N-(3-Methyl-carbamoyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

A solution of compound 458-A (0.41 g, 0.804 mmol) in acetonitrile (12 mL) was treated with diisopropylethylamine (350 μL, 2.01 mmol) and HBTU (0.336 g, 0.885 mmol) and stirred at ambient temperature for 5 min. The resultant solution was split into 3 equal portions. One portion was treated with methylamine (2.0 M in THF, 402 μL, 402 mmol) and stirred for 18 h. The reaction mixture was partitioned between dichloromethane and water, the organic layer dried over sodium sulfate, filtered and the solvent evaporated in vacuo. The crude residue was purified by reverse phase pHPLC (C₁₈), eluting with an acetonitrile (30-90%) in water (0.1% TFA) gradient to afford 73 mg of compound 458 as a colorless solid. ¹H-NMR (CDCl₃): δ 2.96 (d, 2H), 4.47 (br s, 1H), 4.74 (br s, 2H), 7.04 (t, 1H), 7.19-7.32 (m, 1H), 7.32-7.46 (m, 2H), 7.49-7.71 (m, 4H), 7.72-7.84 (m, 1H), 7.85-8.01 (m, 3H); MS: m/z 523.2 (MH⁺).

Following the procedure described above for example 37 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 457 N-(3-Dimethyl-carbamoyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

MS: m/z 537.2 (MH⁺).

Compound 459 N-(3-Carbamoyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 4.77 (br s, 2H), 6.86 (br s, 1H), 7.04 (t, 1H), 7.32-7.48 (m, 3H), 7.52 (dd, 1H), 7.60-7.68 (m, 2H), 7.70-7.80 (m, 3H), 7.90 (d, 2H), 8.02 (d, 1H); MS: m/z 509.1 (MH⁺).

Compound 465 N-(Butyl)-N-(3-carbamoyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 447.1 (MH⁺).

Compound 466 N-(Butyl)-N-(3-methyl-carbamoyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 461.1 (MH⁺).

Compound 467 N-(Butyl)-N-(3-dimethyl-carbamoyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.85 (t, 3H), 1.19-1.37 (m, 2H), 1.43-1.58 (m, 1H), 1.61-1.81 (m, 1H), 2.90 (s, 3H), 3.16 (s, 3H), 3.45 (ddd, 1H), 3.86 (ddd, 1H), 3.98 (s, 3H), 7.34-7.44 (m, 2H), 7.51-7.60 (m, 1H), 7.66-7.75 (m, 1H), 7.90 (d, 2H), 8.19 (d, J=8.67 Hz, 2H); MS: m/z 475.2 (MH⁺).

Example 38

{2-[Benzenesulfonyl-(4-fluoro-3-trifluoromethyl-benzyl)-amino]-benzo[b]thiophen-3-yl}-carbamic acid t-butyl ester (509-A)

A solution of compound 458-A (1.96 g, 3.85 mmol) and diisopropylethylamine (806 μL, 4.61 mmol) in t-butanol (30 mL) was treated with DPPA (1.0 mL, 4.61 mmol) and refluxed for 6 h. The solvent was evaporated in vacuo, and the crude residue purified by flash column chromatography (SiO₂), eluting with an ethyl acetate (10-35%) in heptane gradient, to afford compound 509-A (1.0 g, 45%) as a yellow amorphous solid. ¹H-NMR (CDCl₃): δ 1.48 (br s, 9H), 4.74 (s, 2H), 6.92-7.14 (m, 2H), 7.29-7.39 (m, 2H), 7.43-7.58 (m, 5H), 7.62-7.77 (m, 4H); MS: m/z 603.0 (MNa⁺).

N-(3-Amino-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide (509-B)

Compound 509-A (1.0 g, 1.72 mmol) was dissolved in 4N HCl in dioxane (20 mL) and stirred at ambient temperature for 18 h. The resultant suspension was diluted with diethyl ether, filtered, washed with diethyl ether and dried under vacuo to afford 0.65 g of compound 509-B. MS: m/z 481.0 (MH⁺).

Compound 509 N-{2-[Benzenesulfonyl-(4-fluoro-3-trifluoromethyl-benzyl)-amino]-benzo[b]thiophen-3-yl}-acetamide

A solution of compound 509-B (80 mg, 0.155 mmol) and diisopropylethylamine (68 μL, 0.387 mmol) in dichloromethane, cooled to 0° C., was treated with acety chloride (15 μL, 0.201 mmol) and the resultant solution was stirred at ambient temperature for 18 h. An additional portion of acetyl chloride (15 μL, 0.201 mmol) was added, and the solution was stirred an additional hour. The solution was washed with 2N HCl, saturated aqueous sodium bicarbonate, dried over sodium sulfate, filtered and the solvent evaporated in vacuo. The crude residue was purified by reverse phase pHPLC (C₁₈), eluting with a gradient of acetonitrile (40-90%) in water (0.1% TFA) to afford crude compound 509. Crude compound 509 was further purified by flash column chromatography (SiO₂) eluting with an ethyl acetate (20-70%) in heptane gradient to afford 51 mg of compound 509 an off-white solid. ¹H-NMR (CDCl₃): δ 2.11 (s, 3H), 4.68 (br s, 2H), 6.75-7.08 (m, 1H), 7.11-7.71 (m, 11H), 7.88 (br s, 1H); MS: m/z 523.0 (MH⁺).

Compound 500 N-(3-Acetylamino-benzo[b]thiophen-2-yl)-N-(butyl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 461.1 (MH⁺).

Example 39

Compound 508 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methanesulfonylamino-benzo[b]thiophen-2-yl)-benzenesulfonamide

To a solution of compound 509-B (75 mg, 0.145 mmol) and pyridine (25 μL, 0.304 mmol) in dichloroethane (2 mL), cooled to 0° C., was added a solution of methanesulfonyl chloride 1M in dichloromethane (0.145 mL, 0.145 mmol). After stirring the reaction at ambient temperature for 1 h, pyridine (2 mL) was added and the solution cooled on an ice bath. An additional portion of methanesulfonyl chloride (30 μL) was added, and the solution stirred 4 h at ambient temperature. Diisopropylethylamine (60 mL) was added followed by another portion of methanesulfonyl chloride (30 μL), and the reaction mixture stirred for 2 days. The solution was partitioned between dichloromethane and 2N HCl, dried over sodium sulfate filtered, and the solvent was evaporated in vacuo. The crude residue was purified by reverse phase pHPLC, using a gradient of acetonitrile (40-90%) in water (0.1% TFA) to afford 11 mg of compound 508 as a colorless solid. ¹H-NMR (CDCl₃): δ 2.69 (s, 3H), 4.77 (br s, 2H), 7.11 (t, 1H), 7.35-7.47 (m, 3H), 7.50-7.62 (m, 5H), 7.64-7.73 (m, 3H), 8.02 (d, 1H); MS: m/z 559.0 (MH⁺).

Example 40

Compound 510 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2-carboxy-ethanesulfonamide

A solution of compound 71 (110 mg, 0.225 mmol) in acetic acid (5 mL) and 6N HCl (5 mL) was refluxed for 2 h. The reaction mixture was cooled and the solvent evaporated in vacuo. The crude residue was purified by pHPLC (C18), eluting with an acetonitrile (30-90%) in water (0.1% TFA) gradient, to afford 60 mg of compound 510 as a colorless solid. ¹H-NMR (CDCl₃): δ 2.04 (s, 3H), 2.91-3.04 (m, 2H), 3.48-3.63 (m, 2H), 4.82 (br s, 2H), 7.10 (t, 1H), 7.32-7.42 (m, 2H), 7.42-7.51 (m, 1H), 7.51-7.64 (m, 2H), 7.68-7.82 (m, 1H); MS: m/z 476.1 (MH⁺).

Following the procedure described above for example 40 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 604 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-2-carboxy-ethanesulfonamide

MS: m/z 396.0 (MH⁺).

Compound 605 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-2-carboxy-ethanesulfonamide

MS: m/z 410.1 (MH⁺).

Compound 606 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-2-carboxy-ethanesulfonamide

MS: m/z 424.0 (MH⁺).

Compound 762 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3-trifluoromethoxy-benzyl)-2-carboxy-ethanesulfonamide

¹H-NMR (CDCl₃): δ 2.00 (s, 3H), 2.88-3.06 (m, 2H), 3.55 (t, 2H), 4.81 (br s, 2H), 7.11-7.41 (m, 6H), 7.55-7.62 (m, 1H), 7.70-7.78 (m, 1H); MS: m/z 474.0 (MH⁺).

Compound 795 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-2-carboxy-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.98 (s, 3H), 2.77 (t, 2H), 2.67 (t, 2H), 4.83 (br s, 2H), 7.23-7.35 (m, 2H), 7.35-7.46 (m, 4H), 7.62-7.73 (m, 1H), 7.84-7.96 (m, 1H), 12.57 (br s, 1H); MS: m/z 474.0 (MH⁺).

Example 41

N-(3-Methyl-benzo[b]thiophen-2-yl)-C,C,C-trifluoromethanesulfonamide (662-A)

A solution of compound 757-A (0.25 g, 1.25 mmol) and triethylamine (540 μL, 3.88 mmol) in dichloromethane (10 mL,) cooled to −10° C., was treated with trifluoromethanesulfonic anhydride (442 μL, 2.62 mmol). The reaction mixture was stirred at −10° C. for 1 h, washed with 1N HCl, dried over Na₂SO₄, filtered, and the solvent was evaporated in vacuo to afford crude a bis-sulfonylated by-product. The bis-sulfonylated by-product was dissolved in methanol (4 mL), treated with 4 N NaOH (625 mL, 1.88 mmol) and stirred at ambient temperature for 1 h. The solution was concentrated in vacuo, diluted with H₂O, acidified with 2N HCl, extracted with EtOAc, and the organic phase washed with brine, dried over Na₂SO₄, filtered, and the solvent was evaporated in vacuo to afford 0.35 g of crude compound 662-A

MS: m/z 294.0 (M-H)⁻.

Compound 662 C,C,C-Trifluoro-N-(3-methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-methanesulfonamide

A solution of triphenylphosphine (0.404 g, 1.54 mmol) in THF (10 mL) was treated with DEAD (40% in toluene, 684 μL, 1.54 mmol) and stirred at ambient temperature for 5 min. Compound 662-A (0.35 g) was added and the reaction mixture stirred for 15 min, to which was added 5,5,5-trifluoropentanol (164 μL, 1.42 mmol), and the resultant solution was stirred at ambient temperature for 4 h. The solvent was evaporated in vacuo, and the crude residue purified by flash column chromatography (SiO₂) eluting with an ethyl acetate (1-30%) in heptane gradient to afford crude compound 662. Further purification by pHPLC (C₁₈), eluting with an acetonitrile (40-90%) in water (0.1% TFA) gradient, to afford 0.126 g of compound 662 as an oil. ¹H-NMR (CDCl₃): δ 1.58-1.78 (m, 4H), 1.96-2.18 (m, 2H), 2.42 (s, 3H), 3.73-3.90 (m., 2H), 7.35-7.50 (m, 2H), 7.62-7.83 (m, 2H); MS: m/z 420.0 (MH⁺).

Following the procedure described above for example 41 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 664 C,C,C-Trifluoro-N-(4-fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-methanesulfonamide

MS: m/z 472.0 (MH⁺).

Compound 665 N-(2-Cyclopropyl-ethyl)-C,C,C-trifluoro-N-(3-methyl-benzo[b]thiophen-2-yl)-methanesulfonamide

MS: m/z 364.0 (MH⁺).

Example 42

Compound 663 N-Benzo[b]thiophen-2-yl-N-(4-fluoro-3-trifluoromethyl-benzyl)-C,C,C-trifluoro-methanesulfonamide

A solution of compound 300-A (0.101 g, 0.279 mmol) and triethylamine (86 μL, 0.614 mmol) in dichloromethane (4 mL), cooled to −10° C., was treated with trifluoromethanesulfonic anhydride (52 μL, 0.307 mmol) and stirred at −10° C. for 1 h. The reaction mixture was washed with 2N HCl, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by pHPLC (C₁₈), eluting with an acetonitrile (30-90%)-water gradient, to afford 40 mg of compound 663 as a brown oil. ¹H-NMR (CDCl₃): δ 4.49 (s, 2H), 7.11-7.26 (m, 3H), 7.36 (t, 1H), 7.47-7.68 (m, 4H).

Example 43

(4-Fluoro-3-trifluoromethyl-benzyl)-(3-formyl-benzo[b]thiophen-2-yl)-2,2,2-trifluoro-ethanesulfonamide (704-A)

Compound 704-A was prepared using the procedure in Example 16, step A, substituting compound 1 with compound 697.

Compound 704 N-(3-Hydroxymethyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2,2,2-trifluoro-ethanesulfonamide

A solution of compound 704-A (0.16 g, 0.32 mmol) in THF (5 mL) was treated with lithium borohydride (10 mg, 0.46 mmol) and stirred at ambient temperature for 2 h. The reaction mixture was quenched with H₂O, stirred for 2 h and extracted ethyl acetate. The organic phase was washed with brine, dried over Na₂SO₄, filtered, and the solvent was evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂), eluting with an ethyl acetate (10-50%) in heptane gradient to afford 70 mg of compound 704 as a colorless solid. ¹H-NMR (CDCl₃): δ 2.21 (t, 1H), 4.03 (q, 2H), 4.22 (d, 2H), 4.87 (s, 2H), 7.13 (t, 1H), 7.39-7.54 (m, 4H), 7.76-7.85 (m, 1H), 7.85-8.01 (m, 1H); MS: m/z 484.0 [M-(OH)]⁺, 524.1 (MNa⁺).

Example 44

Compound 699 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-hydroxy-propane sulfonamide

A solution of compound 71 (0.47 g, 0.96 mmol) in THF (5 mL) was treated with lithium borohydride (21 mg, 0.96 mmol) and stirred at ambient temperature for 1 h. An additional portion of lithium borohydride (30 mg, 1.38 mmol) was added and the resultant mixture was stirred at ambient temperature for 2 h. Water (2 mL) was added, the reaction mixture stirred for 5 min and then partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an ethyl acetate (30-100%) in heptane gradient to afford 0.334 g of compound 699 as a colorless oil. ¹H-NMR (CDCl₃): δ 1.61 (t, 1H), 2.06 (s, 3H), 2.11-2.23 (m, 2H), 3.34-3.44 (m, 2H), 3.83 (q, 2H), 4.82 (br s, 2H), 7.09 (t, 1H), 7.34-7.43 (m, 2H), 7.43-7.53 (m, 1H), 7.52-7.65 (m, 2H), 7.69-7.78 (m, 1H); MS: m/z 462.1 (MH⁺).

Following the procedure described above for example 44 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 758 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-hydroxy-butanesulfonamide

¹H-NMR (CDCl₃): δ 1.38 (t, 1H), 1.68-1.82 (m, 2H), 1.97-2.15 (m, 2H) superimposed on 2.09 (s, 3H), 3.20-3.36 (m, 2H), 3.72 (q, 2H), 4.82 (br s, 2H), 7.09 (t, 1H), 7.34-7.42 (m, 2H), 7.44-7.51 (m, 1H), 7.53-7.63 (m, 2H), 7.70-7.77 (m, 1H); MS: m/z 476.1 (MH⁺).

Compound 764 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3-trifluormethoxy-benzyl)-3-hydroxy-propanesulfonamide

¹H-NMR (CDCl₃): δ 1.64 (t, 1H), 2.02 (s, 3H), 2.10-2.25 (m, 2H), 3.29-3.43 (m, 2H), 3.82 (q, 2H), 4.81 (br s, 2H), 7.10-7.41 (m, 6H), 7.59 (dd, 1H), 7.68-7.76 (m, 1H); MS: m/z 460.0 (MH⁺).

Compound 793 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2-hydroxy-ethanesulfonamide

¹H-NMR (CDCl₃): δ 2.04 (s, 3H), 2.45 (t, 1H), 3.41-3.56 (m, 2H), 4.08-4.25 (m, 2H), 4.83 (br s, 2H), 7.10 (t, 1H), 7.34-7.43 (m, 2H), 7.43-7.51 (m, 1H), 7.53-7.64 (m, 2H), 7.69-7.77 (m, 1H); MS: m/z 448.0 (MH⁺).

Example 45

Compound 725 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-hydroxy-3-methyl-butane-1-sulfonamide

A solution of compound 71 (0.11 g, 0.225 mmol) in THF (4 mL) cooled to −10° C., was treated with methylmagnesium bromide (3 M in Et₂O, 2 mL, 6 mmol) and stirred at −10° C. for 1 h. Saturated aqueous ammonium chloride (0.5 mL) was added, the mixture partitioned between H₂O and EtOAc, the organic layer washed with brine, and dried over Na₂SO₄, filtered, and the solvent evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂) eluting with an ethyl acetate (10-60%) in heptane gradient to afford 73 mg of compound 725 as a colorless oil. ¹H-NMR (CDCl₃): δ 1.18-1.33 (br s, 1H) superimposed on 1.30 (s, 6H), 1.98-2.11 (m, 2H) superimposed on 2.06 (s, 3H), 3.33-3.44 (m, 2H), 4.82 (br s, 2H), 7.09 (t, 1H), 7.35-7.42 (m, 2H), 7.44-7.51 (m, 1H), 7.54-7.63 (m, 2H), 7.70-7.77 (m, 1H); MS: m/z 490.0 (MH⁺).

Following the procedure described above for example 45 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 371 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-(1-hydroxy-1-methyl-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.46 (s, 6H), 1.60-1.67 (m, 2H), 2.22 (s, 3H), 2.30-2.39 (m, 2H), 3.16-3.18 (d, 1H), 3.60 (m, 1H), 7.39-7.47 (m, 2H), 7.72 (s, 4H), 7.75-7.80 (m, 1H), 7.82-7.89 (m, 1H); MS: m/z 472.0 (MH⁺).

Compound 374 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-(1-hydroxy-1-methyl-ethyl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.48 (s, 6H), 1.94 (s, 3H), 4.82 (s, 2H), 5.33 (s, 1H), 7.35-7.47 (m, 3H), 7.61-7.87 (m, 8H); MS: m/z 537.9 (MH⁺).

Compound 759 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-hydroxy-4-methyl-pentane-1-sulfonamide

¹H-NMR (CDCl₃): δ 1.23 (s, 1H), 1.26 (s, 6H), 1.57-1.67 (m, 2H), 1.97-2.09 (m, 2H) superimposed on 2.09 (s, 3H), 3.21-3.32 (m, 2H), 4.82 (br s, 2H), 7.09 (t, 1H), 7.35-7.42 (m, 2H), 7.45-7.51 (m, 1H), 7.53-7.63 (m, 2H), 7.67-7.83 (m, 1H); MS: m/z 526.0 (MNa⁺).

Compound 763 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3-trifluoromethoxy-benzyl)-3-hydroxy-3-methyl-butane-1-sulfonamide

¹H-NMR (CDCl₃): δ 1.29 (s, 6H), 1.30 (s, 1H), 1.98-2.10 (m, 2H) superimposed on 2.02 (s, 3H), 3.32-3.45 (m, 2H), 4.81 (br s, 2H), 7.10-7.41 (m, 6H), 7.55-7.62 (m, 1H), 7.73 (dd, 1H); MS: m/z 488.1 (MH⁺).

Compound 796 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-3-hydroxy-3-methyl-butane-1-sulfonamide

¹H-NMR (CDCl₃): δ 1.29 (s, 6H) superimposed on 1.33 (br s, 1H), 1.99 (s, 3H), 2.01-2.09 (m, 2H), 3.26-3.49 (m, 2H), 4.80 (br s, 2H), 7.10 (d, 2H), 7.28-7.41 (m, 4H), 7.53-7.63 (m, 1H), 7.68-7.79 (m, 1H); MS: m/z 488.1 (MH⁺).

Example 46

Compound 769 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3-trifluoromethoxy-benzyl)-3-bromo-propane-1-sulfonamide

A solution of compound 764 (0.80 g, 1.7 mmol) and CBr₄ (0.635 g, 1.92 mmol) in dichloromethane (25 mL) was treated with triphenylphosphine (0.503 g, 1.92 mmol) and stirred at ambient temperature for several hours. Additional portions of CBr₄ (0.20 g, 0.6 mmol) and triphenylphosphine (0.15 g, 0.57 mmol) were added and stirred an additional 18 h. The solvent was evaporated and the crude residue purified by flash column chromatography (SiO₂) eluting with an ethyl acetate (1-25%) in heptane gradient to afford 0.90 g of compound 769 as an oil. ¹H-NMR (CDCl₃): δ 2.02 (s, 3H), 2.39-2.51 (m, 2H), 3.34-3.43 (m, 2H), 3.55 (t, 2H), 4.81 (br s, 2H), 7.10-7.41 (m, 6H), 7.55-7.62 (m, 1H), 7.70-7.77 (m, 1H); MS: m/z 522, 524 (MH⁺).

Following the procedure described above for example 46 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 771 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-bromo-butane-1-sulfonamide

¹H-NMR (CDCl₃): δ 1.98-2.20 (m, 4H) superimposed on 2.04 (s, 3H), 3.17-3.31 (m, 2H), 3.45 (t, 2H), 4.83 (br s, 2H), 7.10 (t, 1H), 7.34-7.43 (m, 2H), 7.44-7.51 (m, 1H), 7.53-7.64 (m, 2H), 7.70-7.78 (m, 1H); MS: m/z 538.0, 540.0 (MH⁺).

Compound 797 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-2-bromo-ethane-1-sulfonamide

¹H-NMR (CDCl₃): δ 1.97-2.11 (m, 3H), 3.62-3.79 (m, 4H), 4.82 (br s, 2H), 7.10 (t, 1H), 7.36-7.51 (m, 3H), 7.54 (dd, 1H), 7.58-7.64 (m, 1H), 7.72-7.79 (m, 1H); MS: m/z 510, 512.0 (MH⁺).

Example 47

Compound 770 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3-trifluoromethoxy-benzyl)-cyclopropanesulfonamide

A solution of compound 769 (90 mg, 0.172 mmol) in DMF (2 mL) was treated with sodium imidazolide (0.10 g, 1.1 mmol), and the resultant mixture was stirred at ambient temperature for 18 h. The solvent was evaporated, and the crude residue pre-absorbed onto silica gel. The product was isolated by flash column chromatography (SiO₂) eluting with an ethyl acetate (5-40%)-heptane gradient to afford 51 mg of compound 770 as an oil. ¹H-NMR (CDCl₃): δ 1.03-1.14 (m, 2H), 1.20-1.32 (m, 2H), 2.05 (s, 3H), 2.61 (tt, 1H), 4.81 (br s, 2H), 7.11 (d, 1H), 7.18-7.31 (m, 3H), 7.31-7.41 (m, 2H), 7.54-7.62 (m, 1H), 7.69-7.76 (m, 1H); MS: m/z 442.0.

Example 48

Compound 779 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-(imidazol-1-yl)-butane-1-sulfonamide

A solution of compound 771 (96 mg, 0.18 mmol) in acetonitrile (1 mL) was treated with imidazole (0.25 g, 3.7 mmol) and heated at 80° C. for 18 h. The solvent was evaporated in vacuo, and the crude residue was purified by pHPLC (C₁₈) eluting with an acetonitrile (20-90%) in water (0.1% TFA) gradient to afford 58 mg of compound 779 as the product as the TFA salt. ¹H-NMR (DMSO-d₆): δ 1.67-1.82 (m, 2H), 1.90-2.06 (m, 2H) superimposed on 2.02 (s, 3H), 3.40-3.61 (m, 2H), 4.27 (t, 2H), 4.86 (br s, 2H), 7.34-7.52 (m, 3H), 7.58-7.76 (m, 4H), 7.81 (t, 1H), 7.84-7.97 (m, 1H), 9.15 (s, 1H); MS: m/z 526.2 (MH⁺).

Following the procedure described above for example 48 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 778 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3-trifluoromethoxy-benzyl)-3-imidazol-1-yl-propane-1-sulfonamide

MS: m/z 510.1 (MH⁺).

Example 49

Compound 724 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-3-oxo-propane-1-sulfonamide

A solution of compound 699 (0.415 g, 0.899 mmol) in dichloromethane (20 mL) was treated with Dess-Martin periodinane (0.57 g, 1.35 mmol) and stirred at ambient temperature for 3 days. The crude residue was preabsorbed onto silica gel and purified by flash column chromatography (SiO₂) eluting with an ethyl acetate (10-60%) in heptane gradient to afford 0.255 g of compound 724 as an oil. ¹H-NMR (CDCl₃): δ 2.04 (s, 3H), 3.11 (t, 2H), 3.55 (t, 2H), 4.81 (br s, 2H), 7.10 (t, 1H), 7.34-7.43 (m, 2H), 7.44-7.51 (m, 1H), 7.53-7.63 (m, 2H), 7.70-7.77 (m, 1H), 9.84 (s, 1H); MS: m/z 460.0.

Example 50

Compound 413 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxamide-benzenesulfonamide

To a pressure vessel containing compound 411 (266 mg; 0.542 mmol) was added methanol (5 mL). The suspension was cooled to 0° C., hydrogen chloride_(g) was bubbled into the suspension for 10 min, the reaction was sealed and allowed to stir at ambient temperature for 2 h. The reaction was cooled, the pressure released, and the solvent evaporated under reduced pressure. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C-18 column; 100×30 mm I.D.; 5 μA) eluting with a 55 to 75% gradient to afford 61 mg of compound 413 as a white solid. MS: m/z 509.0 (MH⁺).

Following the procedure described above for example 50 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 414 N-(Benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-carboxamide-benzene-sulfonamide

MS: m/z 443.0 (MH⁺)

Example 51

4-Benzyloxy-4-[4-fluoro-3-trifluoromethyl-benzyl)-(3-methyl-benzo[b]thiophen-2-yl)-sulfamoyl]-benzamide (555-A)

To a suspension of compound 306 (127.6 mg; 0.244 mmol) in CH₂Cl₂ (1 mL) was added H₂NOBz (60 mg; 0.488 mmol) followed by EDC-HCl (94 mg; 0.488 mmol) and the reaction was allowed to stir at ambient temperature for 5 h. The reaction mixture was diluted with EtOAc, washed with H₂O (2×), brine, dried over Na₂SO₄, filtered and the solvent evaporated under reduced pressure. The crude residue was purified by flash chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford 118.4 mg of compound 555-A as a white solid. ¹H-NMR (DMSO-d₆): δ 1.94 (s, 3H), 4.97 (s, 4H), 7.37-7.49 (m, 8H), 7.64-7.70 (m, 3H), 7.82-7.85 (m, 1H), 7.99 (s, 5H), 12.10 (s, 1H); MS: m/z 629.1 (MH⁺).

Compound 555 4-([4-Fluoro-3-trifluoromethyl-benyzl)-(3-methyl-benzo[b]thiophen-2-yl)-sulfamoyl]-N-hydroxy-benzamide

To a solution of compound 555-A (91.6 mg; 0.175 mmol) in CH₂Cl₂ (2 mL), cooled to 0° C., was added a 1.0M soln of BBr₃-CH₂Cl₂ (0.263 mL) and the reaction was stirred at ambient temperature for 8 h. The solvent was evaporated under reduced pressure and the crude residue purified by reverse-phase semi-prep HPLC (Gemini, C-18 column; 100×30 mm I.D.; 5μ) eluting with a 50% to 70% MeCN—H₂O gradient to afford 46.0 mg of compound 555 as a red oil. ¹H-NMR (DMSO-d₆): δ 1.94 (s, 3H), 4.88 (s, 2H), 7.36-7.40 (m, 2H), 7.43-7.48 (m, 1H), 7.64-7.69 (m, 3H), 7.81-7.86 (m, 1H), 7.95-8.02 (m, 4H), 9.28 (s, 1H), 11.53 (s, 1H); MS: m/z 539.1 (MH⁺).

Example 52

4-Bromo-2-fluoro-N-(3-methyl-benzo[b]thiophen-2-yl)-benzenesulfonamide (589-A)

To a suspension of compound 757-A (1.64 g; 8.23 mmol) in CH₂Cl₂ (10 mL), was added pyridine (1.33 mL; 16.5 mmol) and the reaction was cooled to 5° C. 4-Bromo-2-fluorobenzenesulfonyl chloride (2.5 g; 9.14 mmoL), dissolved in CH₂Cl₂ (5 mL) was added drop-wise, and the reaction was allowed to stir at ambient temperature for 18 h. The reaction was diluted with EtOAc, washed with 1N HCl, water, brine, dried over Na₂SO₄, filtered, and the solvent evaporated under reduced pressure. The crude solid was triturated with CH₂Cl₂-MeOH, filtered, and the solid washed with ether and dried under vacuo to afford 450 mg of compound 589-A as a white solid. The solvent was evaporated and the crude residue dried under vacuo to afford an additional 2.4 g of compound 589-A as a pink solid. MS: m/z 423.9 (MH⁺+MeCN).

2-Fluoro-4-(3-methyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzene-sulfonamide (589-B)

To a solution of compound 589-A (2.46 g; 6.14 mmol), in DMF (30 mL) and MeOH (70 mL), was added TEA (2.57 mL; 18.4 mmol), and (PPh₃)₂PdCl₂ (194 mg). The reaction mixture was added to a high pressure vessel, purged with vacuo and CO (3×). Carbon monoxide was added to the vessel to 50 psi, and the reaction was heated at 80° C. for 18 h. An additional 239 mg of palladium catalyst was added, CO added and the reaction heated at 80° C. for an additional 96 h (convenient—over weekend). The reaction was cooled, the pressure carefully released, and the solvent concentrated under reduced pressure. The crude residue was diluted with EtOAc, washed with H₂O (2×), brine, dried over Na₂SO₄, filtered and the solvent evaporated under reduced pressure. The crude residue was purified by flash chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford 1.12 g of compound 589-B as a yellow foam. ¹H-NMR (DMSO-d₆): δ 2.13 (s, 3H), 3.89 (s, 2H), 7.31-7.38 (m, 2H), 7.64-7.66 (m, 1H), 7.78-7.80 (m, 1H), 7.84-7.89 (m, 2H), 7.95-7.98 (m, 1H), 11.05 (s, 1H); MS: m/z 380.1 (MH⁺).

N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-2-fluoro-4-carbomethoxy-benzenesulfonamide (589-C)

To PPh₃ (155 mg; 0.593 mmol) was added THF (3.5 mL) followed by DEAD (0.275 mL; 0.604 mmol) and the reaction mixture was stirred at RT for 3 min, to which was then added compound 589-B (42 mg; 0.482 mmol). The reaction mixture was stirred for 5 min, to which was added cyclopropyl-ethanol and the reaction was stirred for 72 h. The reaction was diluted with EtOAc, washed with H₂O, brine, dried over Na₂SO₄, filtered and the solvent evaporated under reduced pressure to afford compound 589-C, which was used as is in the next step.

Compound 589 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-2-fluoro-4-carboxy-benzenesulfonamide

To a solution of compound 589-C (˜0.395 mmol) in MeOH (2 mL) was added 3N NaOH (0.198 mL; 0.593 mmol) and the reaction was stirred at 63° C. for 18 h. The reaction was cooled, the solvent evaporated under reduced pressure, and the crude residue partitioned between 1N HCl and EtOAc. The organic layer was washed with H₂O, brine, dried over Na₂SO₄, filtered, and the solvent evaporated under reduced pressure. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C-18 column; 100×30 mm I.D.; 5μ) eluting with a 53 to 73% gradient to afford 109.8 mg of compound 589 as a white solid. ¹H-NMR (DMSO-d₆): δ 0.005-0.03 (t, 3H), 0.366-0.410 (m, 2H), 0.668-0.754 (m, 1H), 1.39-1.40 (m, 2H), 2.23 (s, 3H), 3.77-3.96 (m, 2H), 7.38-7.44 (m, 2H), 7.76-7.88 (m, 4H), 7.96-7.97 (m, 1H), 13.84 (s, 1H); MS: m/z 433.8 (MH⁺).

Following the procedure described above for example 52 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 590 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-2-fluoro-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.25 (s, 3H), 2.51-2.67 (m, 2H), 3.91-4.00 (m, 2H), 7.40-7.46 (m, 2H), 7.76-7.88 (m, 4H), 7.96-7.99 (m, 1H), 13.92 (s, 1H); MS: m/z 461.7 (MH⁺).

Compound 591 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-2-fluoro-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.57 (m, 4H), 2.24 (s, 3H), 3.75 (m, 2H), 7.38-7.45 (m, 2H), 7.76-7.88 (m, 4H), 7.94-7.97 (m, 1H), 13.90 (s, 1H); MS: m/z 489.6 (MH⁺).

Compound 592 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-fluoro-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.90 (s, 3H), 5.00 (m, 2H), 7.35-7.40 (m, 2H), 7.45-7.50 (t, 1H), 7.63-7.69 (m, 3H), 7.82-7.89 (m, 3H), 7.99-8.02 (d, 1H), 13.93 (s, 1H); MS: m/z 541.7 (MH⁺).

Compound 593 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(butyl)-2-fluoro-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.838-0.875 (t, 3H), 1.30-1.39 (m, 2H), 1.42-1.49 (m, 2H), 2.24 (s, 3H), 3.71 (m, 2H), 7.38-7.45 (m, 2H), 7.47-7.87 (m, 4H), 7.94-7.97 (m, 1H), 13.91 (s, 1H); MS: m/z 421.7 (MH⁺).

Compound 638 N-(3-Benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-2-fluoro-4-carboxy-benzenesulfonamide

MS: m/z 419.7 (MH⁺).

Compound 639 N-(3-Benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-2-fluoro-4-carboxy-benzenesulfonamide

MS: m/z 447.7 (MH⁺).

Compound 685 N-(Benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-2-fluoro-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.56-1.60 (m, 4H), 2.22-2.35 (m, 2H), 3.83-3.87 (m, 2H), 7.33-7.39 (m, 3H), 7.77-7.80 (m, 1H), 7.84-7.94 (m, 4H), 13.80 (s, 1H); MS: m/z 476.1 (MH⁺).

Compound 686 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-fluoro-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 5.14 (s, 2H), 7.25 (s, 1H), 7.30-7.35 (m, 2H), 7.47-7.54 (t, 1H), 7.69-7.75 (m, 3H), 7.81-7.88 (m, 1H), 7.91-8.00 (m, 4H), 13.97 (s, 1H); MS: m/z 528.0 (MH⁺).

Compound 774 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-3-fluoro-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.93 (s, 3H), 4.62-4.93 (s, 2H), 7.14-7.16 (m, 2H), 7.23-7.44 (m, 4H), 7.48-7.54 (m, 2H), 7.57-7.67 (m, 2H), 7.85-7.88 (m, 1H), 13.92 (s, 1H); MS: m/z 540.0 (MH⁺).

Compound 775 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-fluoro-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.71-4.86 (m, 2H), 7.36-7.51 (m, 6H), 7.59-7.69 (m, 3H), 7.85-7.88 (m, 1H), 12.84 (s, 1H); MS: m/z 542.1 (MH⁺).

Example 53

Compound 637-A was prepared as per Example 1, step A, substituting 3-methyl-benzo[b]thiophen-2-carboxylic acid for benzo[b]thiophen-2-carboxylic acid, step C, substituting 4-cyanobenzenesulfonyl chloride for benzenesulfonyl chloride, and Example 3, step A, substituting trifluoropropan-1-ol for cyclohexylmethanol.

N-Hydroxy-4-[(3-methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide (637-B)

To a solution of compound 637-A (354 mg; 0.834 mmol) in DMSO (4 mL), purged with N₂, was added hydroxylamine hydrochloride (290 mg; 4.17 mmol) followed by TEA (581 μL; 4.17 mmol) and the reaction was heated under microwave irradiation at 100° C. for 10 min. The reaction was partitioned between H₂O and EtOAc, the layers separated, the organic phase washed with H₂O, brine, dried over MgSO₄, filtered and the solvent evaporated under reduced pressure to afford 410.2 mg of compound 637-B as a white foam. ¹H-NMR (DMSO-d₆): δ 2.23 (s, 3H), 2.52-2.59 (m, 2H), 3.85 (s, 2H), 6.03 (s, 2H), 7.39-7.46 (m, 2H), 7.77-7.80 (m, 3H), 7.86-7.93 (m, 3H), 10.04 (s, 1H); MS: m/z 457.6 (MH⁺).

Compound 637 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)-benzenesulfonamide

A mixture of compound 637-B (403 mg; 0.882 mmol) and TCDI (90%; 259 mg; 1.32 mmol) in THF (3.5 mL) was stirred at rt for 30 min. The reaction was diluted with water and extracted with EtOAc. The extract was washed with H₂O, brine, dried over Na₂SO₄, filtered and the solvent evaporated under reduced pressure to afford an off-white foam. The solid was dissolved in THF (3.5 mL) to which was added boron trifluoride diethyl etherate (332 μL; 2.64 mmol) and the reaction stirred at room temperature for 1 h. The reaction mixture was partitioned between H₂O and EtOAc, the layers separated, the organic phase washed with H₂O, brine, dried over Na₂SO₄, filtered and evaporated under reduced pressure. The solid was triturated with MeOH, filtered, washed to MeOH and dried under vacuo to afford 274 mg of compound 637 as a white solid. ¹H-NMR (DMSO-d₆): δ 2.23 (s, 3H), 2.52-2.59 (m, 2H), 3.89 (s, 2H), 7.40-7.47 (m, 2H), 7.78-7.79 (m, 1H), 7.80-7.82 (m, 1H), 7.85-7.87 (m, 2H), 7.95-8.19 (m, 2H), 13.68 (s, 1H); MS: m/z 499.6 (MH⁺).

Following the procedure described above for example 53 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 640 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.54-1.56 (m, 4H), 2.22-2.31 (m, 5H), 3.63-3.74 (m, 2H), 7.38-7.47 (m, 2H), 7.78-7.80 (m, 1H), 7.81-7.87 (m, 1H), 7.93-7.96 (m, 2H), 8.16-8.19 (m, 2H), 13.70 (s, 1H); MS: m/z 527.7 (MH⁺).

Compound 641 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.000-0.074 (m, 3H), 0.353-0.412 (m, 2H), 0.685-0.751 (m, 1H), 1.35-1.36 (m, 2H), 2.25 (s, 3H), 3.63 (m, 2H), 7.38-7.46 (m, 2H), 7.76-7.82 (m, 1H), 7.83-7.86 (m, 1H), 7.93-7.95 (m, 2H), 8.17-8.19 (m, 1H), 13.69 (s, 1H); MS: m/z 471.7 (MH⁺).

Compound 642 N-(Benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(5-oxo-4,5-dihydro-[1,2,4]-thiadiazol-3-yl)-benzenesulfonamide

MS: m/z 457.7 (MH⁺).

Compound 684 N-(Benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(5-oxo-4,5-dihydro-[1,2,4]-thiadiazol-3-yl)-benzenesulfonamide

MS: m/z 486.0 (MH⁺).

Compound 687 N-(Benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(5-oxo-4,5-dihydro-[1,2,4]-thiadiazol-3-yl)-benzenesulfonamide

MS: m/z 514.0 (MH⁺).

Compound 784 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.95 (s, 3H), 4.87-4.88 (m, 2H), 7.25-7.54 (m, 3H), 7.59-7.68 (m, 4H), 7.83-7.85 (m, 3H), 8.20-8.22 (d, 2H); MS: m/z 580.0 (MH⁺).

Compound 810 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-(5-oxo-4,5-dihydro-[1,2,4]-thiadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.91 (s, 3H), 4.80-4.85 (m, 2H), 7.28-7.34 (m, 2H), 7.35-7.41 (m, 4H), 7.63-7.66 (m, 1H), 7.81-7.84 (m, 3H), 8.20-8.22 (d, 2H); MS: m/z 578.0 (MH⁺).

Example 54

(3-Methyl-benzo[b]thiophen-2-yl)-1H-benzoimidazole-2-sulfonamide

To a suspension of compound 757A (1.89 g; 9.45 mmol) in DCM (20 mL), cooled to 0° C., was added pyridine (1.68 mL; 20.8 mmol), followed by the addition of compound Int-5 (2.2 g; 10.1 mmol) in one-portion. The reaction mixture was allowed to stir at ambient temperature for 4 h, diluted with CH₂Cl₂, washed with H₂O (2×), dried over Na₂SO₄, filtered, the solvent evaporated under reduced pressure and the crude residue purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford 1.72 g of compound 745A as an off-white solid. ¹H-NMR (DMSO-d₆): δ 2.13 (s, 3H), 7.31-7.38 (m, 4H), 7.66-7.68 (m, 2H), 7.77-7.79 (m, 2H), 11.18 (s, 1H), 13.63 (s, 1H); MS: m/z 344.0 (MH⁺).

Compound 726 N-(Cyclopropyl-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-1H-benzimidazole-2-sulfonamide

To PPh₃ (0.462 g; 1.76 mmol) was added THF (10 mL) followed by DEAD (40%; 815 μL; 1.79 mmol) and the reaction mixture was stirred at ambient temperature for 3 min, to which was added compound 745-A (0.403 g; 1.17 mmol). The reaction mixture was stirred for 5 min, to which was added cyclopropyl ethanol (0.123 g; 1.43 mmol) and the reaction was stirred for an additional 18 h. The reaction was diluted with EtOAc, washed with H₂O, brine, dried over Na₂SO₄, filtered and the solvent evaporated under reduced pressure. The crude oil was purified by reverse-phase semi-prep HPLC (Gemini, C-18 column; 100×30 mm I.D.; 5μ) eluting with a 55% to 75% gradient to afford 189 mg of compound 726 as an off-white solid. ¹H-NMR (DMSO-d₆): δ 0.008-0.056 (m, 2H), 0.394-0.438 (m, 2H), 0.727-0.802 (m, 1H), 1.45 (m, 2H), 2.28 (s, 3H), 3.83-3.91 (m, 2H), 7.36-7.57 (m, 4H), 7.77-7.82 (m, 4H), 13.78 (s, 1H); MS: m/z 412.0 (MH⁺).

Compound 745 N-(Cyclopropyl-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-1-methyl-1H-benzimidazole-2-sulfonamide

To a solution of compound 726 (0.125 g; 0.132 mmol) in DMF (2 mL) was added DBU (99 μL; 0.666 mmol) followed by dimethyl sulfate (32 μL; 0.332 mmol) and the reaction was stirred at 67° C. for 18 h. An additional portion of DBU (226 μL; 1.51 mmol) and dimethyl sulfate (144 μL; 1.51 mmol) was added and the reaction mixture was stirred at 67° C. for an additional 18 h. The reaction mixture was cooled, diluted with H₂O, extracted with EtOAc, the layers separated, and the organic phase washed with H₂O, brine, dried over Na₂SO₄, filtered and the solvent evaporated under reduced pressure. The crude oil was purified by reverse-phase semi-prep HPLC (Gemini, C-18 column; 100×30 mm I.D.; 5μ) eluting with a 55% to 75% gradient to afford 107 mg of compound 745 as an oil. ¹H-NMR (DMSO-d₆): δ 0.008-0.013 (m, 2H), 0.346-0.391 (m, 2H), 0.685-0.759 (m, 1H), 1.43 (m, 2H), 2.31 (s, 3H), 3.79 (s, 3H), 3.84-3.97 (m, 2H), 7.33-7.38 (m, 3H), 7.39-7.49 (m, 1H), 7.69-7.72 (d, 1H), 7.75-7.81 (m, 2H), 7.88-7.90 (d, 1H); MS: m/z 426.1 (MH⁺).

Following the procedure described above for example 54 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 720 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-1H-benzimidazole-2-sulfonamide

¹H-NMR (DMSO-d₆): δ 1.48-1.75 (m, 4H), 2.13-2.27 (m, 5H), 3.40-387 (m, 2H), 7.37-7.47 (m, 4H), 7.60-7.83 (m, 4H), 13.83 (s, 1H); MS: m/z 468.1 (MH⁺).

Compound 722 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-1-methyl-1H-benzimidazole-2-sulfonamide

MS: m/z 534.2 (MH⁺).

Compound 728 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-1H-benzimidazole-2-sulfonamide

MS: m/z 520.0 (MH⁺).

Compound 729 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-1H-benzimidazole-2-sulfonamide

MS: m/z 518.1 (MH⁺).

Compound 746 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-1-methyl-1H-benzimidazole-2-sulfonamide

MS: m/z 532.0 (MH⁺).

Example 55

(3-Methyl-benzo[b]thiophen-2-yl)-1H-benzimidazole-2-sulfonamide (727-A)

To a suspension of compound 757-A (0.589 g; 2.95 mmol) in DCM (20 mL), cooled to 0° C., was added pyridine (525 μL; 6.49 mmol), followed by the addition of compound Int-7 (0.5 g; 1.88 mmol) in one-portion. The reaction was allowed to stir at ambient temperature for 4 h, diluted with CH₂Cl₂, washed with H₂O (2×), dried over Na₂SO₄, filtered, the solvent evaporated under reduced pressure and the crude residue purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford crude compound 727-A. Compound 727-A was further purified by reverse-phase semi-prep HPLC (Gemini, C-18 column; 100×30 mm I.D.; 5μ) eluting with a 60% to 80% gradient to afford 131 mg of compound 727-A as a white solid. MS: m/z 392.0 (MH⁺).

Compound 727 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5,-trifluoro-pentyl)-1H-benzimidazole-2-sulfonamide

To PPh₃ (0.068 g; 0.258 mmol) was added THF (1.5 mL) followed by DEAD (40%; 120 μL; 0.263 mmol) and the reaction mixture was stirred at ambient temperature for 3 min, to which was then added compound 727-A (0.067 g; 0.172 mmol). The reaction mixture was stirred for 5 min, to which was added 5,5,5-trifluoro-pentan-1-ol (0.03 g; 0.210 mmol) and the reaction was stirred for an additional 18 h. The reaction mixture was diluted with EtOAc, washed with H₂O, brine, dried over Na₂SO₄, filtered and the solvent evaporated under reduced pressure. The crude oil was purified by reverse-phase semi-prep HPLC (Gemini, C-18 column; 100×30 mm I.D.; 5μ) eluting with a 65% to 85% gradient to afford 34 mg of compound 727 as a white solid. MS: m/z 516.2 (MH⁺).

Example 56

Compound 811-A, was prepared by the method used to synthesize compound 600 in Example 30, steps A and B.

4-[(3-Methyl-benzo[b]thiophen-2-yl)-(5,5,5-trifluoro-pentyl)-sulfamoyl)]-benzimidic acid ethyl ester (811-B)

To a solution of compound 811-A (706 mg; 1.56 mmol), cooled to 0° C. was bubbled HCl(g) for 15 min. The reaction was sealed and allowed to stir 18 h at ambient temperature. The solvent was evaporated under reduced pressure and the solid dried to afford 777 mg of compound 811-B as a white solid.

(Ethoxy-{4-[(3-methyl-benzo[b]thiophen-2-yl)-(5,5,5-trifluoro-pentyl)-sulfamoyl]-phenyl}-methylene)-carbamic acid methyl ester (811-C)

To a suspension of compound 811-B (777 mg; 1.45 mmol), in CHCl₃ (1 mL), was added 2,4,6-collidine (275 μL; 1.93 mmol), followed by methyl chloroformate (115 μL; 2.18 mmol) and the reaction was stirred at ambient temperature for 72 h. TEA (200 μL) was added to the reaction, followed by another 1.5 equiv of methyl chloroformate and the reaction was stirred at ambient temperature for 18 h. The reaction was diluted with CH₂Cl₂, washed with H₂O, dried over Na₂SO₄, filtered, and the solvent evaporated under reduced pressure to afford crude compound 811-C.

Compound 811 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(5-oxo-4,5-dihydro-1H-[1,2,4]triazol-3-yl)-benzenesulfonamide

To a solution of compound 811-C (403 mg; 0.775 mmol), in carbontetrachloride (3.5 mL), was added hydrazine (25 μL; 797 mmol) and the reaction was refluxed in a sealed tube for 18 h. The reaction was cooled and the solvent evaporated. The crude reaction was purified by reverse-phase semi-prep HPLC (Gemini, C-18 column; 100×30 mm I.D.; 5μ) eluting with a 50 to 70% gradient to afford 75 mg of compound 811 as a white solid. ¹H-NMR (DMSO-d₆): δ 1.52-1.55 (m, 4H), 2.19-2.22 (m, 5H), 3.50-3.69 (m, 2H), 7.39-7.46 (m, 2H), 7.78-7.79 (m, 1H), 7.80-7.90 (m, 3H), 8.00-8.02 (d, 2H), 11.97 (s, 1H), 12.29 (s, 1H); MS: m/z 511.0 (MH⁺).

Compound 812 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(1-methyl-5-oxo-4,5-dihydro-1H-[1,2,4]triazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.36-1.40 (m, 4H), 1.92-2.06 (m, 5H), 3.23 (s, 3H), 3.28-3.42 (m, 2H), 7.22-7.29 (m, 2H), 7.61-7.62 (m, 1H), 7.63-7.70 (m, 1H), 7.72-7.74 (d, 2H), 7.83-7.85 (d, 2H), 12.32 (s, 1H); MS: m/z 525.0 (MH⁺).

Example 57

Compound 789 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-dimethylamino-3-pyridylsulfonamide

To a solution of compound 789-A (0.07 g, 0.14 mmol) in DMSO (1 mL) was added a solution of 2.0 M dimethylamine-tetrahydrofuran (0.205 mL, 0.41 mmol) and the reaction mixture was stirred at ambient temperature for 18 h. The crude reaction was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.06 g of compound 789 as a white solid. ¹H NMR (DMSO-d₆) δ 1.98 (s, 3H), 3.16 (s, 6H), 4.72 (br s, 2H), 6.79 (d, 1H), 7.28 (d, 2H), 7.33-7.47 (m, 4H), 7.60-7.71 (m, 1H), 7.76-7.94 (m, 2H), 8.42 (d, 1H); MS: m/z 522.2 (MH⁺).

Following the procedure described above for example 57 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 786 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-dimethylamino-3-pyridyl-sulfonamide

¹H-NMR (DMSO-d₆): δ −0.10-0.07 (m, 2H), 0.27-0.47 (m, 2H), 0.61-0.82 (m, 1H), 1.34 (br s, 2H), 2.31 (s, 3H), 3.16 (s, 6H), 3.40-3.67 (m, 2H), 6.78 (d, 1H), 7.34-7.55 (m, 2H), 7.67-7.85 (m, 2H), 7.85-7.96 (m, 1H), 8.34 (d, 1H); MS: m/z 416.1 (MH⁺).

Compound 787 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-dimethylamino-3-pyridyl-sulfonamide

¹H-NMR (DMSO-d₆) δ 1.51 (br s, 4H), 2.30 (s, 6H), 2.4-2.5 (m, 2H), 3.14 (s, 6H), 6.76 (d, 1H), 7.32-7.52 (m, 2H), 7.72 (dd, 1H), 7.79 (dd, 1H), 7.88 (dd, 1H), 8.34 (d, 1H); MS: m/z 472.0 (MH⁺).

Compound 788 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-morpholino-3-pyridyl-sulfonamide

¹H NMR (DMSO-d₆): δ 1.51 (br s, 5H), 2.31 (s, 6H), 3.57 (s, 2H), 3.61-3.82 (m, 9H), 6.97 (d, 1H), 7.35-7.56 (m, 2H), 7.69-7.84 (m, 2H), 7.84-7.94 (m, 1H), 8.39 (d, 1H); MS: m/z 514.0 (MH⁺).

Compound 790 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-morpholino-3-pyridyl-sulfonamide

¹H NMR (DMSO-d₆): δ 1.99 (s, 3H), 3.65-3.87 (m, 8H), 4.72 (br s, 2H), 7.00 (d, 1H), 7.29 (d, 2H), 7.33-7.50 (m, 4H), 7.60-7.74 (m, 1H), 7.79-7.94 (m, 2H), 8.46 (d, 1H); MS: m/z 564.0 (MH⁺).

Compound 798 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-morpholino-3-pyridyl-sulfonamide

MS: m/z 451.8 (MH⁺).

Example 58

Compound 357 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-methoxy-pyridin-3-ylsulfonamide

To a solution of compound 77 (0.07 g, 0.14 mmol) in toluene (1 mL) was added a solution of 0.5M solution of sodium methoxide in MeOH (0.82 mL, 0.41 mmol) and the reaction mixture was refluxed for 2 h. The reaction mixture was cooled, diluted with H₂O, extracted with EtOAc, washed with H₂O, brine, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.06 g of compound 357 as a white solid. ¹H-NMR (CDCl₃) δ 1.78-1.97 (s, 3H), 4.23 (s, 3H), 5.02 (br s, 2H), 6.93 (dd, 1H), 7.10 (t, 1H), 7.30-7.36 (m, 2H), 7.42-7.67 (m, 4H), 8.00 (dd, 1H), 8.38 (dd, 1H); MS: m/z 510.9 (MH⁺).

Following the procedure described above for example 58 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 358 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-dimethylamino-pyridin-3-yl-sulfonamide

¹H-NMR (CDCl₃) δ 1.88 (s, 3H), 3.07 (s, 6H), 4.95 (br s, 2H), 6.93 (dd, 1H), 7.07 (t, 1H), 7.28-7.36 (m, 2H), 7.37-7.47 (m, 1H), 7.47-7.55 (m, 2H), 7.55-7.62 (m, 1H), 8.02 (dd, 1H), 8.47 (dd, 1H); MS: m/z 524.0 (MH⁺).

Compound 359 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methoxy-pyridin-3-yl-sulfonamide

¹H-NMR (CDCl₃) δ 2.04-2.15 (m, 3H), 4.05 (s, 3H), 4.68 (br s, 2H), 6.85 (d, 1H), 7.07 (t, 1H), 7.30-7.50 (m, 3H), 7.50-7.75 (m, 3H), 7.88 (dd, 1H), 8.62 (d, 1H); MS: m/z 510.9 (MH⁺).

Compound 360 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-dimethylamino-pyridin-3-yl-sulfonamide

MS: m/z 524.0 (MH⁺).

Compound 377 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-2-thiomethyl-pyridin-3-yl-sulfonamide

MS: m/z 527.0 (MH⁺).

Compound 378 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-thiomethyl-pyridin-3-yl-sulfonamide

MS: m/z 527.0 (MH⁺).

Compound 448 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(butyl)-2-dimethylamino-pyridin-3-yl-sulfonamide

¹H-NMR (CDCl₃) δ 0.89 (t, 3H), 1.37 (m, 2H), 1.45-1.62 (m, 2H), 2.38 (s, 3H), 3.17 (s, 6H), 3.72 (m., 2H), 6.99 (dd, 1H), 7.37 (m, 2H), 7.59-7.80 (m, 2H), 8.14-8.29 (m, 1H), 8.37-8.50 (m, 1H); MS: m/z 404.1 (MH⁺).

Example 59

Compound 428-A, was prepared by the method used to synthesize compound 600 in Example 30, steps A and B.

Compound 428 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

Dimethylformamide (2 mL), sodium azide (0.098 g, 1.5 mmol), ammonium chloride (0.08 g, 1.5 mmol) and compound 428-A (0.185 g, 0.5 mmol) were added to a microwave vessel with stir bar, sealed, and heated in a 300 watt microwave reactor to 160° C. for 10 min. The solution was decanted, N-bromosuccinimide (0.356 g, 2.0 mmol) was added to the solution and stirred for 3 h at ambient temperature. The solution was diluted with H₂O, extracted with EtOAc, washed with H₂O, brine, dried over Na₂SO₄, filtered, and the solvent was evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.124 g of compound 428 as a white solid. ¹H-NMR (CD₃OD) δ 0.91 (t, 3H), 1.48 (tt, 4H), 3.74 (t, 2H), 7.35-7.59 (m, 2H), 7.73-7.88 (m, 2H), 7.93 (m, 2H), 8.26 (m, 2H); MS: m/z 492.0 (MH⁺).

Following the procedure described above for example 59 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 424 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 4.98 (s, 2H), 7.16 (s, 1H), 7.25-7.29 (m, 2H), 7.41-7.46 (t, 1H), 7.65-7.69 (m, 3H), 7.76-7.79 (m, 1H), 8.00-8.02 (d, 2H), 8.24-8.26 (d, 2H); MS: m/z 534.0 (MH⁺).

Compound 425 N-(Benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

MS: m/z 468.0 (MH⁺).

Compound 429 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-butyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (CD₃OD) δ 1.82 (br s, 2H), 2.41 (br s, 2H), 3.83 (s, 2H), 7.44-7.60 (m, 2H), 7.77-7.89 (m, 2H), 7.93 (m, 2H), 8.27 (m, 2H); MS: m/z 546.0 (MH⁺).

Compound 449 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

MS: m/z 414.0 (MH⁺).

Compound 455 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-(1H-tetrazol-5-yl)-benzenesulfonamide

MS: m/z 548.0 (MH⁺).

Compound 474 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclopropyl-methyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 0.05-0.17 (m, 2H), 0.38 (d, 2H), 0.90 (br s, 1H), 3.55 (br s, 2H), 7.40-7.63 (m, 2H), 7.72-7.81 (m, 1H), 7.85 (m, 2H), 7.94-8.08 (m, 1H), 8.20 (m, 2H); MS: m/z 490.0 (MH⁺).

Compound 475 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 4.92 (br s, 2H), 7.35-7.54 (m, 3H), 7.60-7.80 (m, 3H), 7.85-8.03 (m, 3H), 8.24 (d, 2H); MS: m/z 612.0 (MH⁺).

Compound 539 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(butyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (CDCl₃) δ 0.89 (t, 3H), 1.28-1.45 (m, 2H), 1.45-1.59 (m, 2H), 2.39 (s, 3H), 3.54 (s, 2H), 7.30-7.48 (m, 2H), 7.58-7.77 (m, 2H), 7.93 (m, 2H), 8.27 (m, 2H); MS: m/z 428.1 (MH⁺).

Compound 542 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.07 (s, 3H), 3.53 (br s, 2H), 7.01-7.14 (m, 1H), 7.30-7.41 (m, 2H), 7.45 (dd, 1H), 7.55 (dd, 1H), 7.57-7.68 (m, 2H), 7.98 (m, 2H), 8.34 (m, 2H); MS: m/z 548.1 (MH⁺).

Compound 569 N-(Benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

MS: m/z 425.7 (MH⁺).

Compound 570 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ −0.12-0.09 (m, 2H), 0.25-0.47 (m, 2H), 0.59-0.84 (m, 1H), 1.34 (br s, 2H), 2.26 (s, 3H), 3.62 (br s, 2H), 7.31-7.51 (m, 2H), 7.69-7.83 (m, 3H), 7.83-7.92 (m, 1H), 8.20 (d, 2H); MS: m/z 440.1 (MH⁺).

Compound 571 N-(Benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

MS: m/z 453.7 (MH⁺).

Compound 572 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.25 (s, 3H), 2.51-2.67 (m, 2H), 3.90 (m, 2H), 7.40-7.47 (m, 2H), 7.78-7.82 (dd, 1H), 7.84-7.88 (m, 1H), 8.02-8.04 (d, 2H), 8.28-8.30 (d, 2H); MS: m/z 467.7 (MH⁺).

Compound 579 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.56 (d, 4H), 2.10-2.33 (m, 2H), 3.71 (br s, 2H), 7.43-7.60 (m, 2H), 7.72-7.85 (m, 1H), 7.94-8.06 (m, 1H), 8.09 (m, 2H), 8.31 (m, 2H); MS: m/z 561.6 (MH⁺).

Compound 580 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(1H-tetrazol-5-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.41-1.69 (m, 4H), 2.15-2.36 (m, 2H), 3.66 (t, 2H), 7.42-7.64 (m, 2H), 7.74-7.92 (m, 3H), 7.94-8.09 (m, 1H), 8.21 (d, 2H); MS: m/z 516.0 (MH⁺).

Compound 804 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(1H-tetrazol-5-yl)-pyridin-3-ylsulfonamide

Compound 804 was prepared using the procedure in Example 59, step A, substituting compound 428-A with compound Int-9. ¹H-NMR (DMSO-d₆) δ −0.01 (q, 2H), 0.22-0.45 (m, 2H), 0.57-0.80 (m, 1H), 1.37 (br s, 2H), 2.27 (s, 3H), 3.67 (br s, 2H), 7.31-7.53 (m, 2H), 7.79 (dd, 1H), 7.81-7.93 (m, 1H), 8.33-8.57 (m, 2H), 9.04 (d, 1H); MS: m/z 441.0 (MH⁺).

Compound 805 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-(1H-tetrazol-5-yl)-pyridin-3-ylsulfonamide

Compound 805 was prepared using the procedure in Example 59, step A, substituting compound 428-A with compound Int-9. ¹H-NMR (DMSO-d₆) δ 1.83-2.01 (m, 3H), 4.88 (br s, 2H), 7.32 (d, 2H), 7.34-7.52 (m, 4H), 7.61-7.74 (m, 1H), 7.80-7.96 (m, 1H), 8.50 (d, 1H), 8.57 (dd, 1H), 9.18 (d, 1H); MS: m/z 547.0 (MH⁺).

Compound 806 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(1H-tetrazol-5-yl)-pyridin-3-ylsulfonamide

Compound 806 was prepared using the procedure in Example 59, step A, substituting compound 428-A with compound LMR-2-B. ¹H-NMR (DMSO-d₆) δ 1.45 (d, 5H), 2.10 (br s, 3H), 2.13-2.22 (m, 3H), 7.16-7.42 (m, 2H), 7.71 (dd, 1H), 7.77 (dd, 1H), 8.24-8.44 (m, 2H), 8.97 (d, 1H); MS: m/z 497.1 (MH⁺).

Example 60

Compound 514-A, was prepared by the method used to synthesize compound 600 in Example 30, steps A and B.

N-(Benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-N-hydroxy-benzamidine sulfonamide (514-B)

Compound 514-A (1.0 g, 2.7 mmol), triethylamine (1.88 mL, 13.5 mmol), hydroxylamine hydrochloride (0.938 g, 13.5 mmol), and dimethylsulfoxide (4 mL) were added to a microwave vessel with stir bar, sealed and heated in a 300 watt microwave reactor to 160° C. for 10 min. The solids were rinsed with DMSO, filtered, the organic washes diluted with H₂O, extracted with EtOAc, washed with H₂O, brine, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo. Crude compound 514-B crystallized to afford 1.0 g of an off white solid. MS: m/z 458.0 (MH⁺).

Compound 513 N-(Benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

To an ice-cooled solution of pyridine (0.10 mL, 1.24 mmol) and compound 514-B (0.50 g, 1.24 mmol), sealed in a microwave vessel, under N₂, was added 2-ethylhexylchloroformate (0.239 g, 1.24 mmol), drop-wise. The reaction mixture was stirred at 0° C. for 30 mins and heated at 140° C. for 30 min in a 300 watt microwave. The solution was diluted with H₂O, extracted with EtOAc, washed with H₂O, brine, Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 50 to afford 0.175 g of compound 513 as a white solid. ¹H-NMR (DMSO-d₆) δ 1.66-1.82 (m, 2H), 2.26-2.45 (m, 2H), 3.78 (t, 2H), 7.25-7.37 (m, 1H), 7.37-7.46 (m, 2H), 7.77-7.84 (m, 1H), 7.86-7.93 (m, 1H), 7.96 (m, 2H), 8.04 (m, 2H), 13.21 (br s, 1H); MS: m/z 484.1 (MH⁺).

Compound 514 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

N-Bromosuccinimide (0.037 g, 0.21 mmol) was added to a solution of dichloroethane (2 mL), and compound 513 (0.10 g, 0.21 mmol) and the reaction mixture was stirred at ambient temperature for 18 h. The solution was diluted with H₂O, extracted with EtOAc, washed with H₂O, brine, Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.024 g of compound 514 as a white solid. ¹H-NMR (DMSO-d₆): δ1.60-1.79 (m, 2H), 2.24-2.45 (m, 2H), 3.68-3.83 (m, 2H), 7.45-7.66 (m, 2H), 7.69-7.92 (m, 1H), 7.92-8.17 (m, 5H), 13.25 (br s, 1H); MS: m/z 562.8 (MH⁺).

Following the procedure described above for example 60 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 442 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

MS: m/z 430.0 (MH⁺).

Compound 443 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (CD₃OD) δ 0.91 (t, 3H), 1.32-1.60 (m, 4H), 3.63-3.83 (m, 2H), 7.46-7.62 (m, 2H), 7.74-7.88 (m, 2H), 7.90 (m, 2H), 8.00 (s, 2H), 8.06 (m, 2H); MS: m/z 507.9 (MH⁺).

Compound 471 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-4-N-hydroxy-benzamidinesulfonamide

MS: m/z 404.1 (MH⁺).

Compound 473 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-4-N-hydroxy-benzamidinesulfonamide

¹H-NMR (DMSO-d₆) δ 0.73-0.89 (m, 3H), 1.30-1.46 (m, 4H), 3.64 (br s, 2H), 7.46-7.61 (m, 3H), 7.74-7.84 (m, 1H), 7.92 (d, 2H), 7.97-8.03 (m, 1H), 8.09 (d, 2H), 8.24 (s, 1H); MS: m/z 484.4 (MH⁺).

Compound 482 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-N-hydroxy-benzamidinesulfonamide

¹H-NMR (DMSO-d₆) δ 5.03 (s, 2H), 7.19 (s, 1H), 7.29-7.38 (m, 2H), 7.50 (t, 1H), 7.66-7.78 (m, 3H), 7.78-7.88 (m, 1H), 7.95 (s, 4H); MS: m/z 524.5 (MH⁺).

Compound 483 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 5.03 (s, 2H), 7.21 (s, 1H), 7.26-7.39 (m, 2H), 7.41-7.59 (m, 1H), 7.62-7.78 (m, 3H), 7.78-7.93 (m, 1H), 7.98-8.16 (m, 4H), 13.24 (br s, 1H); MS: m/z 550.1 (MH⁺).

Compound 511 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (CDCl₃) δ 4.91 (s, 2H), 7.05-7.17 (m, 1H), 7.35-7.48 (m, 2H), 7.48-7.57 (m, 2H), 7.71 (dd, 2H), 7.95 (m, 2H), 8.03 (m, 2H); MS: m/z 628.0 (MH⁺).

Compound 512 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

Compound 512 was synthesized as per compound 514 of Example 60, substituting NBS with NCS. ¹H-NMR (CDCl₃) δ 4.89 (s, 2H), 7.12 (d, 1H), 7.39-7.48 (m, 2H), 7.53 (d, 2H), 7.63-7.76 (m, 2H), 7.94 (m, 2H), 8.03 (m, 2H); MS: m/z 584.0 (MH⁺).

Compound 515 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

Compound 515 was synthesized as per compound 514 of Example 60, substituting NBS with NCS. MS: m/z 515.8 (MH⁺).

Compound 541 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(butyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (CDCl₃) δ 0.89 (t, 3H), 1.31-1.44 (m, 2H), 1.5-1.6 (m, 2H), 2.40 (s, 3H), 3.55 (br s, 2H), 7.31-7.49 (m, 2H), 7.58-7.79 (m, 2H), 7.84-8.04 (m, 4H), 10.72 (s, 1H); MS: m/z 444.1 (MH⁺).

Compound 544 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.02-2.19 (m, 3H), 4.76 (br s, 2H), 7.08 (t, 1H), 7.34-7.41 (m, 2H), 7.42-7.48 (m, 1H), 7.54 (dd, 1H), 7.58-7.68 (m, 2H), 7.99 (m, 4H), 11.25 (br s, 1H); MS: m/z 564.0 (MH⁺).

Compound 583 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.40-1.68 (m, 4H), 2.12-2.34 (m, 2H), 3.70 (br s, 2H), 7.39-7.64 (m, 2H), 7.64-7.86 (m, 1H), 7.98-8.04 (m, 1H), 8.07 (s, 4H), 13.24 (br s, 1H); MS: m/z 577.6 (MH⁺).

Compound 584 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

Compound 584 was synthesized as per compound 514 of Example 60, substituting NBS with NCS. ¹H-NMR (DMSO-d₆) δ 1.57-1.62 (m 4H) 2.18-2.39 (m, 2H) 3.57-3.86 (m, 2H) 7.46-7.65 (m, 2H) 7.68-7.87 (m, 1H) 7.98-8.04 (m, 1H) 8.07 (s, 4H) 13.24 (br s, 1H); MS: m/z 531.6 (MH⁺).

Compound 597 N-(Benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

MS: m/z 496.6 (MH⁺).

Compound 599 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 2.24 (s, 3H), 2.54-2.63 (m, 2H), 3.88 (br s, 2H), 7.35-7.56 (m, 2H), 7.78-7.83 (m, 1H), 7.84-7.90 (m, 1H), 7.99-8.08 (m, 4H), 13.23 (br s, 1H); MS: m/z 483.6 (MH⁺).

Compound 608 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 2.54-2.77 (m, 2H), 4.00 (t, 2H), 7.44-7.64 (m, 2H), 7.68-7.85 (m, 1H), 7.94-8.21 (m, 5H), 13.25 (br s, 1H); MS: m/z 549.6 (MH⁺).

Compound 609 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(5-oxo-4,5-dihydro-[1,2,4]-oxadiazol-3-yl)-benzenesulfonamide

Compound 609 was synthesized as per compound 514 of Example 60, substituting NBS with NCS. MS: m/z 503.7 (MH⁺).

Compound 612 N-(Benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

MS: m/z 441.7 (MH⁺).

Compound 613 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 0.1-0.2 (m, 2H), 0.4-0.48 (m, 2H), 0.52-0.77 (m, 1H), 1.36 (br s, 2H), 2.26 (s, 3H), 3.65 (br s, 2H), 7.26-7.55 (m, 2H), 7.74-7.82 (m, 1H), 7.82-7.89 (m, 1H), 8.00 (m, 2H), 8.06 (m, 2H), 13.24 (br s, 1H); MS: m/z 455.7 (MH⁺).

Compound 626 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 0.1-0.2 (m, 2H), 0.30-0.54 (m, 2H), 0.69-0.91 (m, 1H), 1.39 (br s, 2H), 3.64-3.89 (m, 2H), 7.55 (dd, 2H), 7.70-7.93 (m, 1H), 7.94-8.24 (m, 5H), 13.25 (br s, 1H); MS: m/z 520.1 (MH⁺).

Compound 627 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

Compound 627 was synthesized as per compound 514 of Example 60, substituting NBS with NCS. ¹H-NMR (DMSO-d₆) δ 0.1-0.2 (m, 2H), 0.26-0.43 (m, 2H,) 0.69-0.80 (m, 1H), 1.38 (q, 2H), 3.73 (t, 2H), 7.47-7.61 (m, 2H,) 7.68-7.85 (m, 1H), 7.89-8.18 (m, 5H), 13.25 (br s, 1H); MS: m/z 476.6 (MH⁺).

Compound 801 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.92 (s, 3H), 4.83 (br s, 2H), 7.26-7.35 (m, 2H), 7.35-7.45 (m, 4H), 7.63-7.72 (m, 1H), 7.83 (dd, 1H), 8.09 (s, 4H), 13.27 (br s, 1H); MS: m/z 562.0 (MH⁺).

Compound 807 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-pyrid-3-ylsulfonamide

Compound 807 was prepared using the procedure in Example 60, step A, substituting compound 514-A with compound Int-9. ¹H-NMR (DMSO-d₆) δ −0.16-0.13 (m, 2H), 0.23-0.46 (m, 2H), 0.72 (br s, 1H), 1.3-1.4 (m, 2H), 3.61 (br s, 2H), 7.29-7.54 (m, 2H), 7.81 (dd, 1H), 7.88 (dd, 1H), 8.24 (d, 1H), 8.46 (dd, 1H), 9.02 (d, 1H), 13.49 (s, 1H); MS: m/z 457.0 (MH⁺).

Compound 808 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-pyrid-3-ylsulfonamide

Compound 808 was prepared using the procedure in Example 60, step A, substituting compound 514-A with compound Int-9. ¹H-NMR (DMSO-d₆) δ 1.79-2.08 (m, 3H,) 4.90 sa (br s, 2H), 7.32 (d, 2H), 7.35-7.48 (m, 4H), 7.59-7.78 (m, 1H), 7.78-7.91 (m, 1H), 8.27 (d, 1H), 8.53 (dd, 1H), 9.14 (d, 1H), 13.46-13.57 (m, 1H); MS: m/z 563.0 (MH⁺).

Compound 809 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(5-oxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-pyrid-3-ylsulfonamide

Compound 809 was prepared using the procedure in Example 60, step A, substituting compound 514-A with compound Int-9. ¹H-NMR (DMSO-d₆) δ 1.43-1.63 (m, 5H), 2.24 (br s, 3H), 2.27-2.37 (m, 3H), 7.30-7.57 (m, 2H), 7.82 (dd, 1H), 7.87-8.00 (m, 1H), 8.24 (d, 1H), 8.46 (dd, 1H), 9.04 (d, 1H), 13.49 (br s, 1H); MS: m/z 513.0 (MH⁺).

Example 61

Compound 472 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-4-N-hydroxyacetyl-benzamidine sulfonamide

A solution of compound 514-B (0.5 g 1.24 mmol), DCM (5 mL), acetic anhydride (0.126 g 1.24 mmol), and triethylamine (0.125 g 1.24 mmol) was stirred at ambient temperature for 18 h. The solution was diluted with H₂O, extracted with EtOAc, washed with H₂O, brine, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.340 g of compound 472 as a white solid. MS: m/z 446.1 (MH⁺).

N-Benzo[b]thiophen-2-yl-N-(butyl)-4-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide (481-B)

To an ice-cooled mixture of compound 472 (0.220 g, 0.494 mmol) and carbon disulfide (0.113 mL, 1.88 mmol) in DMF was added sodium hydride (0.036 g, 1.48 mmol) and the reaction mixture was stirred at 0° C. and allowed to warm to ambient temperature over 18 h. The reaction mixture was diluted with 1N hydrochloric acid, the aqueous phase extracted with EtOAc, washed with H₂O, brine, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.110 g of compound 481-B as a pale, yellow solid. ¹H-NMR (DMSO-d₆) δ 0.86 (t, 3H), 1.25-1.42 (m, 2H), 1.42-1.58 (m, 2H), 3.68 (t, 4H), 7.25 (s, 1H), 7.29-7.45 (m, 2H), 7.72-7.83 (m, 1H), 7.83-7.94 (m, 3H), 8.08 (d, 2H); MS: m/z 446.1 (MH⁺).

Compound 481 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-4-(5-thioxo-4,5-dihydro-[1,2,4]oxadiazol-3-yl)-benzenesulfonamide

N-Bromosuccinimide (0.048, 0.27 mmol) was added to a solution of dichloroethane (2 mL), dimethylformamide (2 mL) and compound 481-B (0.120 g, 0.27 mmol) and stirred at ambient temperature for 18 h. The reaction mixture was diluted with H₂O, the aqueous phase extracted with EtOAc, washed with H₂O, brine, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.019 g of compound 481 pale, pink solid. ¹H-NMR (DMSO-d₆) δ 0.83 (t, 3H), 1.24-1.51 (m, 4H), 3.66 (br s, 3H), 7.44-7.60 (m, 2H), 7.69-7.83 (m, 1H), 7.94-8.07 (m, 3H), 8.07-8.21 (m, 2H); MS: m/z 525.1 (MH⁺).

Example 62

Compound 470 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

To an ice-cooled solution of compound 514-B (0.250 g, 0.62 mmol), pyridine (0.098 g, 1.24 mmol) and THF (4 mL) was added, drop-wise, a solution of thionyl chloride (0.073 g, 0.62 mmol) in DCM (1 mL), and the resulting mixture was stirred for 30 min at 0° C. The solvent was evaporated in vacuo, the residue dissolved in water and extracted with CHCl₃. The solvent was evaporated in vacuo and the crude residue purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.224 g of compound 470 as a white solid. MS: m/z 450.0 (MH⁺).

Compound 484 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

To a solution of compound 470 (0.130 g, 0.289 mmol), DCE (2 mL), and DMF (2 mL) was added N-bromosuccinimide (0.051 g, 0.289 mmol) and the reaction mixture was stirred at ambient temperature for 18 h. The reaction mixture was washed with H₂O, the organics separated, and the solvent was evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.084 g of compound 484 as a white solid. ¹H-NMR (DMSO-d₆) δ 0.73-0.93 (m, 3H), 1.27-1.53 (m, 4H), 3.59-3.81 (m, 2H), 7.44-7.62 (m, 2H), 7.73-7.85 (m, 1H), 7.93-8.07 (m, 3H), 8.07-8.21 (m, 2H); MS: m/z 529.4 (MH⁺).

Following the procedure described above for example 62 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 485 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(butyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

Compound 485 was synthesized as per compound 484 of Example 62, substituting NBS with NCS. ¹H-NMR (DMSO-d₆) δ 0.75-0.91 (m, 3H), 1.26-1.52 (m, 4H), 3.67 (t, 2H), 7.45-7.61 (m, 2H), 7.75-7.89 (m, 1H), 7.95-8.07 (m, 3H), 8.07-8.20 (m, 2H); MS: m/z 485.4 (MH⁺).

Compound 540 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(butyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

¹H-NMR (CDCl₃) δ 0.89 (t, 3H), 1.28-1.44 (m, 2H), 1.44-1.59 (m, 2H), 2.38 (s, 3H), 3.51 (s, 2H), 7.30-7.46 (m, 2H), 7.60-7.76 (m, 2H), 7.78-7.91 (m, 3H), 7.99 (s, 1H); MS: m/z 464.1 (MH⁺).

Compound 543 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

¹H-NMR (CDCl₃) δ 2.02-2.12 (s, 3H), 4.67 (br s, 2H), 7.08 (t, 1H), 7.31-7.38 (m, 2H), 7.44 (dt, 1H), 7.49-7.57 (m, 1H), 7.57-7.73 (m, 2H), 7.82-7.99 (m, 4H); MS: m/z 548.1 (MH⁺).

Compound 581 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.57 (m, 4H), 2.10-2.36 (m, 2H), 3.71 (br s, 2H), 7.43-7.66 (m, 2H), 7.74-7.85 (m, 1H), 7.94-8.09 (m, 3H), 8.09-8.21 (m, 2H); MS: m/z 597.1 (MH⁺).

Compound 582 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

Compound 582 was synthesized as per compound 484 of Example 62, substituting NBS with NCS. MS: m/z 551.5 (MH⁺).

Compound 596 N-(Benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

MS: m/z 489.6 (MH⁺).

Compound 598 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 2.15-2.30 (s, 3H), 2.54-2.64 (m, 2H), 3.41 (br s, 2H), 7.36-7.53 (m, 2H), 7.75-7.83 (m, 1H), 7.83-7.94 (m, 1H), 8.00 (m, 2H), 8.10 (m, 2H); MS: m/z 503.7 (MH⁺).

Compound 607 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

MS: m/z 569.9 (MH⁺).

Compound 610 N-(Benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

MS: m/z 461.7 (MH⁺).

Compound 611 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 0.1-0.2 (m, 2H) 0.28-0.43 (m, 2H) 0.70 (d, 1H) 1.36 (br s, 2H) 2.26 (s, 3H) 3.64 (br s, 2H) 7.28-7.51 (m, 2H) 7.70-7.83 (m, 1H) 7.83-7.93 (m, 1H) 7.99 (d, 2H) 8.04-8.19 (m, 2H); MS: m/z 475.6 (MH⁺).

Compound 624 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 0.1-0.2 (m, 2H), 0.29-0.46 (m, 2H), 0.63-0.86 (m, 1H), 1.38 (q, 2H), 3.74 (t, 2H), 7.44-7.62 (m, 2H), 7.71-7.84 (m, 1H), 7.93-8.07 (m, 3H), 8.07-8.20 (m, 2H); MS: m/z 539.4 (MH⁺).

Compound 625 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(3H-[1,2,3,5]oxathiadiazole-2-oxide)-benzenesulfonamide

Compound 625 was synthesized as per compound 484 of Example 62, substituting NBS with NCS. ¹H-NMR (DMSO-d₆) δ 0.1-0.2 (m, 2H) 0.29-0.43 (m, 2H) 0.68-0.83 (m, 1H) 1.38 (q, 2H) 3.74 (t, 2H) 7.47-7.60 (m, 2H) 7.72-7.87 (m, 1H) 7.96-8.07 (m, 3H) 8.07-8.18 (m, 2H); MS: m/z 495.5 (MH⁺).

Example 63

Compound 559-A, was prepared by the method used to synthesize compound 600 in Example 30, steps A and B.

Compound 446 N-Benzo[b]thiophen-2-yl-N-(butyl)-4-morpholin-4-yl-benzenesulfonamide. Compound 559-A

(0.10 g, 0.236 mmol), 1.0 M potassium t-butoxide-THF (1.41 mL, 1.41 mmol), Pd(dba) (0.01 g, 0.011 mmol), 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthine, (0.006 g, 0.011 mmol), morpholine (0.04 mL, 0.47 mmol) and dioxane (4 mL) were added to a microwave vessel with stir bar and heated at 100° C. for 30 min in a 300 watt microwave reactor. The reaction mixture was diluted with H₂O, extracted with EtOAc, and the solvent evaporated under reduced pressure. The crude residue was dissolved in acetonitrile, the solution filtered and purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.021 g of compound 446 as a dark, viscous oil. ¹H-NMR (CDCl₃) δ 0.89 (t, 3H), 1.29-1.46 (m, 2H), 1.50-1.63 (m, 2H), 3.23-3.34 (m, 4H), 3.57 (t, 2H), 3.81-3.93 (m, 4H), 6.84 (m, 2H), 7.13 (s, 1H), 7.29-7.40 (m, 2H), 7.57 (m, 2H), 7.63-7.73 (m, 2H); MS: m/z 431.1 (MH⁺).

Compound 559 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-4-morpholine-benzenesulfonamide

N-Bromosuccinimide (0.030 g, 0.167 mmol) was added to a solution of dichloroethane (2 mL), and compound 446 (0.072 g, 0.167 mmol) and stirred at ambient temperature for 2 h. The reaction mixture was diluted with H₂O, extracted with EtOAc, and the solvent evaporated under reduced pressure. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.050 g of compound 559 as a dark, green gum. ¹H-NMR (CDCl₃): δ 0.86 (t, 3H), 1.29-1.45 (m, 2H), 1.45-1.59 (m, 2H), 3.23-3.38 (m, 4H), 3.60 (t, 2H), 3.82-3.98 (m, 4H), 6.78-6.95 (m, 2H), 7.34-7.49 (m, 2H), 7.63-7.75 (m, 3H), 7.75-7.84 (m, 1H); MS: m/z 511.0 (MH⁺).

Following the procedure described above for example 63 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 444 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-4-dimethylamino-benzenesulfonamide

MS: m/z 389.1 (MH⁺).

Compound 445 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-4-pyrrolidin-1-yl-benzenesulfonamide

MS: m/z 415.0 (MH⁺).

Compound 447 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-4-(4-methyl-piperazin-1-yl)-benzenesulfonamide

MS: m/z 444.1 (MH⁺).

Compound 560 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-4-dimethylamino-benzenesulfonamide

MS: m/z 467.0 (MH⁺).

Compound 561 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(butyl)-4-dimethylamino-benzenesulfonamide

Compound 561 was synthesized as per compound 559 of Example 63, substituting NBS with NCS. ¹H-NMR (CDCl₃) δ 0.86 (t, 3H) 1.28-1.44 (m, 2H) 1.44-1.55 (m, 2H) 3.06 (s, 6H) 3.57 (t, 2H) 6.65 (m, 2H) 7.35-7.50 (m, 2H) 7.65 (m, 2H) 7.67-7.74 (m, 1H) 7.75-7.86 (m, 1H); MS: m/z 423.0 (MH⁺).

Compound 562 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(butyl)-4-morph olin-4-yl-benzenesulfonamide

Compound 562 was synthesized as per compound 559 of Example 63, substituting NBS with NCS. MS: m/z 465.0 (MH⁺).

Compound 738 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-dimethylamino-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ −0.11-0.05 (m, 2H), 0.31-0.46 (m, 2H), 0.59-0.81 (m, 1H), 1.34 (br s, 2H), 2.31 (s, 3H), 3.08 (s, 6H), 3.52 (br s, 2H), 6.76-6.93 (m, 2H), 7.35-7.51 (m, 2H), 7.51-7.63 (m, 2H), 7.73-7.84 (m, 1H), 7.84-7.97 (m, 1H); MS: m/z 415.2 (MH⁺).

Compound 739 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-diethylamino-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ −0.11-0.06 (m, 2H), 0.31-0.50 (m, 2H), 0.62-0.80 (m, 1H), 1.36 (br s, 2H), 2.27 (s, 3H), 3.01 (br s, 4H), 3.62 (br s, 3H), 3.80 (br s, 3H), 3.98 (s, 1H), 7.36-7.58 (m, 2H), 7.65-7.76 (m, 2H), 7.76-7.84 (m, 1H), 7.84-7.98 (m, 3H); MS: m/z 443.3 (MH⁺).

Compound 740 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-thiomorpholin-4-yl-benzenesulfonamide

MS: m/z 473.2 (MH⁺).

Compound 741 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-mor pholino-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ −0.09-0.11 (m, 2H), 0.26-0.47 (m, 2H), 0.72 (d, 1H), 1.34 (br s, 2H), 2.19-2.35 (m, 3H), 3.24-3.44 (m, 4H), 3.53 (br s, 2H), 3.69-3.89 (m, 4H), 7.12 (d, 2H), 7.36-7.50 (m, 2H), 7.52-7.66 (m, 2H), 7.75-7.86 (m, 1H), 7.86-7.97 (m, 1H); MS: m/z 457.2 (MH⁺).

Compound 742 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-(piperazin-1-yl)-benzenesulfonamide

MS: m/z 456.2 (MH⁺).

Compound 748 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-dimethylamino-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.49 (br s, 4H), 2.27 (s, 6H), 3.03 (s, 6H), 6.79 (d, 2H), 7.32-7.46 (m, 2H), 7.46-7.55 (m, 2H), 7.73-7.82 (m, 1H), 7.84-7.93 (m, 1H); MS: m/z 471.2 (MH⁺).

Compound 749 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-thiomorpholin-4-yl-benzenesulfonamide

MS: m/z 526.2 (MH⁺).

Compound 750 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-morpholino-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.35-1.64 (m, 4H), 2.13-2.35 (m, 5H), 2.99 (br s, 2H), 3.21-3.39 (m, 4H), 3.48 (br s, 2H), 3.53 (br s, 2H), 3.67-3.91 (m, 4H), 7.07 (d, 2H), 7.33-7.52 (m, 2H), 7.56 (d, 2H), 7.78 (dd, 1H), 7.83-8.00 (m, 1H); MS: m/z 513.2 (MH⁺).

Compound 751 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropyl-ethyl)-4-piperidin-1-yl-benzenesulfonamide

MS: m/z 455.2 (MH⁺).

Compound 752 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-piperidine-benzenesulfonamide

MS: m/z 511.16 (MH⁺).

Example 64

Compound 799-A, was prepared by the method used to synthesize compound 757 in Example 29, steps A and B.

Compound 799 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-dimethylamino-benzenesulfonamide

To a solution of compound 799-A (0.07 g, 0.14 mmol) in dimethylsulfoxide (2 mL) was added a 2.0 M solution of dimethylamine-THF (0.42 mmol), the reaction mixture was sealed and heated at 100° C. in a 300 W microwave. The crude solution was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.053 g of compound 799 as an off-white solid. ¹H-NMR (DMSO-d₆) δ 1.96 (s, 3H), 3.05 (s, 6H), 4.65 (br s, 2H), 6.76-6.87 (m, 2H), 7.27 (d, 2H), 7.31-7.45 (m, 4H), 7.52-7.62 (m, 2H), 7.62-7.70 (m, 1H), 7.76-7.91 (m, 1H); MS: m/z 521.1 (MH⁺).

Following the procedure described above for example 64 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 800 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-morpholino-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.96 (s, 3H), 3.24-3.39 (m, 4H) 3.65-3.85 (m, 4H), 4.68 (br s, 2H), 7.11 (d, 2H), 7.28 (d, 2H), 7.32-7.46 (m, 4H), 7.58-7.73 (m, 3H), 7.76-7.89 (m, 1H); MS: m/z 563.1 (MH⁺).

Example 65

Compound 623 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methanesulfonylaminocarbonyl-benzenesulfonamide

To a solution of compound 306 (0.50 g, 0.96 mmol) in THF (30 mL) was added CDI (0.232 g, 1.43 mmol) and the reaction mixture was refluxed for 5 h. Methyl sulfonamide (0.136 g, 1.43 mmol), DBU (0.218 g, 1.43 mmol) and DMAP (0.012 g, 0.096 mmol) were added to the reaction mixture and the reaction was refluxed for 1 h. The solution was diluted with H₂O, extracted with EtOAc, washed with brine, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.2 g of compound 623 as a white solid. ¹H-NMR (DMSO-d₆) δ 1.93 (s, 3H), 3.40 (s, 3H), 4.91 (br s, 2H), 7.34-7.43 (m, 2H), 7.47 (t, 1H), 7.57-7.75 (m, 3H), 7.75-7.89 (m, 1H), 8.02 (m, 2H), 8.18 (m, 2H); MS: m/z 601.0 (MH⁺).

Example 66

Compound 701-A, was prepared by the method used to synthesize compound 757 in Example 29, steps A and B.

Compound 701 4-(2-Dimethylaminomethyl-imidazol-1-yl)-N-(3-methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-benzenesulfonamide

A solution of compound 701-A (0.250 g, 0.414 mmol), DMSO (3 mL), CuI (0.016 g, 0.083 mmol), and K₂CO₃ (0.115 g, 0.828 mmol) was stirred at ambient temperature for 15 min. Compound Int-16 (0.078 g, 0.628 mmol) was added, the reaction mixture refluxed for 18 h, cooled to ambient temperature, and partitioned between H₂O and EtOAc. The aqueous phase was extracted with chloroform, the organics combined, dried over MgSO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.10 g of compound 701 as a yellow oil. ¹H-NMR (DMSO-d₆) δ 1.89-2.01 (m, 3H), 2.80 (s, 5H), 3.17 (s, 3H), 4.49 (s, 2H), 4.85 (br s, 2H), 7.32 (d, 3H), 7.36-7.50 (m, 4H), 7.69 (dd, 1H), 7.75 (s, 1H), 7.80-7.91 (m, 3H), 8.01-8.15 (m, 2H); MS: m/z 601.2 (MH⁺).

Example 67

N-Indan-2-yl-phthalamic acid (747-B)

To a solution of compound 747-A (1.5 g, 11.3 mmol) in CHCl₃ (100 mL) was added phthalic anhydride (2.25 g, 15.2 mmol) and the reaction mixture was heated at 70° C. for 18 h. The reaction mixture was cooled, the solvent evaporated under reduced pressure, H₂O added to the residue, and the residue was extracted with EtOAc, the organic extracts combined, and concentrated in vacuo. The crude residue was triturated with MeOH, the solid filtered and dried under vacuo to afford 2.0 g of compound 747-B as an amber, crystalline solid. MS: m/z 282.1 (MH⁺).

2-Indan-2-yl-isoindole-1,3-dione (747-C)

To a solution of compound 747-B (1.8 g, 0.74 mmol) in DMF (20 mL) was added DMAP (0.782 g; 0.74 mmol) and the reaction mixture was heated at 120° C. for 18 h. The reaction mixture was cooled, diluted with H₂O, and the precipitate filtered and dried under vacuo to afford 1.2 g of compound 747-C as a light brown solid. ¹H-NMR (CDCl₃) δ 3.18 (dd, 2H), 3.63 (dd, 2H), 5.16 (q, 1H), 7.14-7.24 (m, 4H), 7.68-7.77 (m, 2H), 7.79-7.90 (m, 2H); MS: m/z 264.1 (MH⁺).

2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-indan-5-sulfonyl chloride (747-D)

To a solution of compound 747-C (0.72 g, 2.7 mmol) in MeCN (50 mL) was added chlorosulfonic acid (3.72 g, 32.4 mmol), drop-wise, and the reaction mixture was stirred at ambient temperature for 48 h. The reaction mixture was diluted with H₂O, extracted with CH₂Cl₂, dried over Na₂SO₄, filtered, and dried to afford 0.976 g of compound 747-D as a brown solid. ¹H-NMR (CDCl₃) δ 3.26-3.43 (m, 2H,) 3.60-3.78 (m, 2H), 5.26 (t, 1H), 7.46 (d, 1H), 7.68-7.79 (m, 2H), 7.79-7.93 (m, 4H); MS: m/z 384.1 (MNa⁺).

2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-indan-N-(3-methyl-benzo[b]thiophen-2-yl)-N-sulfonamide (747-E)

To a solution of compound 757-A (0.449 g, 2.25 mmol) in DCM (5 mL) and pyridine (0.355 g, 4.5 mmol), cooled to 0° C., was added compound 747-D (0.976 g; 2.7 mmol) in DCM (2 mL) and the reaction mixture was stirred at ambient temperature for 48 h. The reaction mixture was diluted with H₂O, extracted with EtOAc, washed with brine, dried over Na₂SO₄, filtered and the solvent evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.73 g of compound 747-E as a brown solid. MS: m/z 489.1 (MH⁺).

2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-indan-N-(3-methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-N-sulfonamide (747-F)

To a solution of compound 747-E (0.73 g, 1.49 mmol) in DMF (10 mL) was added K₂CO₃ (0.248 g; 1.79 mmol) and the reaction mixture was stirred for 30 min. A solution of 4-fluoro-3-trifluoromethylbenzyl bromide (0.460 g, 1.79 mmol) in DMF (2 mL) was added drop-wise and the reaction mixture stirred at ambient temperature for 18 h. The reaction mixture was diluted with H₂O, extracted with EtOAc, washed with brine, dried over Na₂SO₄, filtered and the solvent was evaporated in vacuo to afford 0.94 g of crude compound 747-F as a white solid. ¹H-NMR (DMSO-d₆) δ 1.99 (s, 3H), 3.47 (m, 4H), 4.86 (br s, 2H), 5.14 (s, 1H), 7.31-7.56 (m, 4H), 7.58-7.75 (m, 4H), 7.79 (s, 1H), 7.82-7.99 (m, 5H); MS: m/z 665.1 (MH⁺). MS: m/z 663.1 (MH⁺).

Compound 747 2-Amino-indan-N-(3-methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-N-sulfonamide

Compound 747-F (0.91 g, 1.37 mmol) was added a 0.2M hydrazine-methanol solution (20 mL) and the reaction mixture was stirred for 2 h at ambient temperature. The solvent was evaporated in vacuo and the crude residue purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.4 g of compound 747 as an orange gum. ¹H-NMR (DMSO-d₆) δ 1.78-1.92 (m, 3H), 2.85-3.03 (m, 2H), 3.22-3.43 (m, 2H), 4.00 (br s, 1H), 4.71 (br s, 2H), 7.20-7.42 (m, 3H), 7.42-7.65 (m, 5H), 7.65-7.81 (m, 2H), 7.97 (br s, 2H); MS: m/z 535.1 (MH⁺).

Example 68

Compound 767 2-Methyl-N-(4-fluoro-3-trifluoromethyl-benzyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-1,2,3,4-tetrahydroisoquinolin-7-yl-sulfonamide

To compound 79 (0.10 g, 0.19 mmol) was added 37% aqueous formaldehyde (0.3 mL) and concentrated formic acid (0.4 mL) and the reaction mixture was heated at 50° C. for 7 days. The reaction mixture was cooled, diluted with H₂O, extracted with EtOAc, washed with brine, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo. The crude residue was purified by reverse-phase semi-prep HPLC (Gemini, C₁₈ column; 100×30 mm I.D.; 5μ) to afford 0.02 g of compound 767 as a clear, viscous oil. ¹H-NMR (DMSO-d₆) δ 1.83-2.02 (m, 3H), 2.96 (s, 3H), 3.13-3.29 (m, 2H), 3.41 (br s, 1H), 3.73 (br s, 1H), 4.40 (br s, 1H), 4.62 (br s, 1H), 4.84 (br s, 2H), 7.33-7.44 (m, 2H), 7.48 (t, 1H), 7.59 (d, 1H), 7.61-7.74 (m, 3H), 7.74-7.92 (m, 3H); MS: m/z 549.2 (MH⁺).

Example 69

N-(3-Methylbenzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide (398-A)

To a stirred solution of compound 757-A (4.99 g, 25.0 mmol) in pyridine (50 mL) and methylene chloride (25 mL), cooled on an ice bath, was added 4-(chlorosulfonyl)benzoic acid (5.52 g, 25.0 mmol), portion-wise, for 4 min, and the reaction was allowed to stir at ambient temperature for 4 days. The reaction mixture was concentrated under reduced pressure, the residue stirred with 1N HCl (100 mL), the resulting solid filtered, washed with 1N HCl and air dried. The crude product was triturated with MeOH (15 mL), filtered, rinsed with MeOH (2×5 mL) and air-dried to afford crude benzoic acid (not shown). The benzoic acid was suspended in MeOH (100 mL), treated with concentrated H₂SO₄ (0.1 mL) and the reaction mixture refluxed for 5 days. The reaction mixture was cooled, the solvent evaporated under reduced pressure, and the residue was triturated with MeOH (15 mL), filtered, washed with methanol (2×5 mL) and once with another portion of methanol (10 mL). The solid was dried to afford 6.31 g of compound 398-A as a tan-yellow powder. ¹H-NMR (DMSO-d₆) δ: 2.02 (s, 3H), 3.89 (s, 3H), 7.40-7.29 (m, 2H), 7.67-7.61 (m, 1H), 7.83-7.77 (m, 1H), 7.89 (d, 2H), 8.14 (d, 2H), 10.66 (s, 1H); MS: m/z 360.2 (M-H⁺).

N-(Butyl)-N-(3-methylbenzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide (398-B)

To a solution of triphenyl phosphine (0.396 g, 1.51 mmol) in THF (10 mL) was added 40% DEAD in toluene solution (0.67 mL, 1.51 mmol) and the reaction mixture was stirred at ambient temperature for 2 min. Compound 398-A (0.361 g, 1.00 mmol) was added in one-portion and the reaction stirred for an additional 5 min. n-Butanol (0.11 mL, 1.20 mmol) was added and the reaction mixture was stirred for 18 h at ambient temperature. The reaction mixture was concentrated under reduced pressure and the crude material purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 0.372 g of compound 398-B as a viscous, colorless oil. ¹H-NMR (DMSO-d₆) δ: 0.84 (t, 3H), 1.48-1.27 (m, 4H), 2.24 (s, 3H), 3.57 (s, 2H), 3.92 (s, 3H), 7.48-7.37 (m, 2H), 7.82-7.76 (m, 1H), 7.88-7.83 (m, 1H), 7.93 (d, 2H), 8.17 (d, 2H); MS: m/z 418.3 (MH⁺).

Compound 398 Sodium, N-(Butyl)-N-(3-methylbenzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

To a solution of compound 398-B (0.371 g, 0.89 mmol) in a 5:1 THF/water mixture (10 mL) was added LiOH.H₂O (0.042 g, 1.00 mmol), the reaction mixture was stirred for 18 h, and the organics were evaporated in vacuo. The crude residue was diluted with H₂O (10 mL), acidified with 1N HCl (1.00 mL), the solid filtered, washed with H₂O and dried under vacuum. The benzoic acid (0.337 g, 0.84 mmol) was dissolved in a mixture of H₂O (10 mL) and 1N NaOH (0.84 mL, 0.84 mmol), with gentle heating. The turbid solution was filtered, frozen and lyophilized to afford 0.359 g of the sodium salt of compound 398 as an off-white solid. ¹H-NMR (DMSO-d₆) δ: 0.83 (t, 3H), 1.43-1.27 (m, 4H), 2.24 (s, 3H), 3.51 (br s, 2H), 7.45-7.37 (m, 2H), 7.64 (d, 2H), 7.79-7.75 (m, 1H), 7.87-7.83 (m, 1H), 7.99 (d, 2H); MS: m/z 402.3 (M-H)⁻.

Following the procedure described above for example 69 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 399 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(cyclopropylmethyl)-4-carboxy-benzenesulfonamide

MS: m/z 401.9 (MH⁺).

Compound 400 Sodium, N-(2-Cyclopropylethyl)-N-(3-methylbenzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.01-0.06 (m, 2H), 0.40-0.32 (m, 2H), 0.74-0.63 (m, 1H), 1.38-1.26 (br m, 2H), 2.23 (s, 3H), 3.58 (br s, 2H), 7.45-7.36 (m, 2H), 7.63 (d, 2H), 7.79-7.74 (m, 1H), 7.87-7.83 (m, 1H), 7.98 (d, 2H); MS: m/z 414.2 (M-H)⁻.

Compound 401 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(2-tert-butoxy-ethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 0.91-1.14 (m, 9H), 2.22 (s, 3H), 3.22-3.49 (m, 4H), 7.34-7.51 (m, 2H), 7.71-7.83 (m, 1H), 7.83-7.89 (m, 1H), 7.92 (m, 2H), 8.14 (m, 2H); MS: m/z 447.9 (MH⁺).

Compound 402 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(ethyl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 389.9 (MH⁺).

Compound 403 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(ethyl)-4-carboxy-benzenesulfonamide

MS: m/z 375.9 (MH⁺).

Compound 404 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(propyl)-4-carboxy-benzenesulfonamide

MS: m/z 398.9 (MH⁺).

Compound 409 Sodium, N-(3-Methylbenzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.22 (s, 3H), 2.58-2.45 (m, 2H), 3.81 (br s, 2H), 7.46-7.37 (m, 2H), 7.66 (d, 2H), 7.81-7.75 (m, 1H), 7.89-7.83 (m, 1H), 8.00 (d, 2H); MS: m/z 442.2 (M-H)⁻.

Compound 410 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.68 (q, 2H), 2.23 (s, 3H), 2.29-2.45 (m, 2H), 3.67 (br s, 2H), 7.28-7.57 (m, 2H), 7.71-8.02 (m, 4H), 8.16 (d, 2H), 13.62 (br s, 1H); MS: m/z 458.0 (MH⁺).

Compound 416 N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(3-tert-butoxy-propyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.08 (s, 9H), 1.59 (t, 2H), 2.26 (s, 3H), 3.21-3.43 (m, 2H), 3.67 (br s, 2H), 3.92 (s, 3H), 7.31-7.54 (m, 2H), 7.79 (dd, 1H), 7.82-7.89 (m, 1H), 7.92 (m, 2H), 8.18 (m, 2H); MS: m/z 476.0 (MH⁺).

Compound 477 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(butyl)-4-carboxy-benzenesulfonamide

¹H NMR (DMSO-d₆) δ 0.71-0.93 (m, 3H), 1.23-1.50 (m, 4H), 3.58 (t, 2H), 7.43-7.64 (m, 2H), 7.72 (d, 2H), 7.77-7.88 (m, 1H), 7.94-8.13 (m, 3H); MS: m/z 423.9 (MH⁺).

Compound 478 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(cyclopropylmethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ −0.14-0.07 (m, 2H), 0.19-0.39 (m, 2H), 0.67-0.94 (m, 1H), 3.40 (d, 2H), 7.33-7.55 (m, 2H), 7.64 (d, 2H), 7.68-7.82 (m, 1H), 7.82-8.07 (m, 3H); MS: m/z 421.8 (MH⁺).

Compound 479 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-2-(cyclopropyl)ethyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ −0.01 (q, 2H), 0.22-0.45 (m, 2H), 0.64-0.84 (m, 1H), 1.34 (q, 2H), 3.66 (t, 2H), 7.46-7.64 (m, 2H), 7.67-7.90 (m, 3H), 7.91-8.17 (m, 3H); MS: m/z 435.9 (MH⁺).

Compound 480 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 2.54-2.70 (m, 2H), 3.90 (t, 2H), 7.45-7.61 (m, 2H), 7.74 (d, 2H), 7.79 (dd, 1H), 7.96-8.17 (m, 3H); MS: m/z 464.0 (MH⁺).

Compound 530 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 491.9 (MH⁺).

Compound 531 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-carbomethoxy-benzenesulfonamide

MS: m/z 506.0 (MH⁺).

Compound 537 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4,4,4-trifluoro-butyl)-4-carboxy-benzenesulfonamide

¹H NMR (DMSO-d₆) δ 1.67 (q, 2H), 2.26-2.45 (m, 2H), 3.68 (t, 2H), 7.48-7.61 (m, 2H), 7.73 (d, 2H), 7.78-7.92 (m, 1H), 7.94-8.13 (m, 3H); MS: m/z 477.9 (MH⁺).

Compound 538 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆) δ 1.35-1.70 (m, 4H), 2.07-2.36 (m, 2H), 3.62 (t, 2H), 7.45-7.63 (m, 2H), 7.73 (d, 2H), 7.76-7.86 (m, 1H), 7.92-8.14 (m, 3H); MS: m/z 492.0 (MH⁺).

Compound 545 Sodium, N-(3-Methylbenzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.62-1.45 (m, 4H), 2.32-2.17 (m, 5H), 3.56 (br s, 2H), 7.45-7.37 (m, 2H), 7.66 (d, 2H), 7.80-7.75 (m, 1H), 7.88-7.83 (m, 1H), 8.00 (m, 2H); MS: m/z 470.2 (M-H)⁻.

Example 70

N-(Benzo[b]thiophen-2-yl)-4-bromobenzenesulfonamide (361-A)

To a stirred solution of compound 1-C (9.28 g, 49.9 mmol) in pyridine (100 mL) and methylene chloride (50 mL), cooled on an ice bath, was added 4-bromobenzene-1-sulfonyl chloride (12.8 g, 49.9 mmol), portion-wise over a period of 4 minutes. The reaction mixture was allowed to warm to ambient temperature and stirred for 18 h. The reaction mixture was concentrated under reduced pressure, the crude residue partitioned between EtOAc (500 mL) and 1N HCl (250 mL), the layers separated, the organic phase washed with 1N HCl (125 mL), brine, dried over MgSO₄, filtered and evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an EtOAc-Heptane gradient to afford 13.5 g of compound 361-A as a tan powder. ¹H-NMR (DMSO-d₆) δ: 6.89 (s, 1H), 7.33-7.20 (m, 2H), 7.75-7.64 (m, 3H), 7.84-7.76 (m, 3H), 11.30 (s, 1H); MS: m/z 366.1 (M-H)⁻.

N-(3-Acetyl-benzo[b]thiophen-2-yl)-4-bromobenzenesulfonamide (361-B)

To a suspension of compound 361-A (9.21 g, 25.0 mmol) in DCM (50 mL), cooled in an ice-bath, was added an ice-cold solution of acetyl chloride (2.30 mL, 32.3 mmol), followed by SnCl₄ (27.9 mmol) in DCM (200 mL). The reaction mixture was allowed to warm to ambient temperature and stirred for 18 h. The reaction mixture was quenched with saturated NH₄Cl solution (125 mL), filtered over a pad of celite, dried over MgSO₄, filtered and concentrated under vacuum. The residue was dissolved in refluxing EtOAc (75 mL), filtered hot and the filtrate allowed to cool. The solid was filtered and washed EtOAc (10 mL). Another batch of product was obtained by evaporation of the mother liquor, dissolving the residue in refluxing EtOAc (25 mL), filtering hot and allowing the filtrate to cool. The solid was filtered and washed with EtOAc (2 mL). The combined batches of solid were air-dried to afford 8.54 g of compound 361-B as a tan-orange powder. ¹H-NMR (DMSO-d₆) δ: 2.57 (s, 3H), 7.40-7.24 (m, 2H), 7.83-7.70 (m, 5H), 8.14 (d, 1H); MS: m/z 408.1 (M-H)⁻.

Compound 386 N-(3-Acetyl-benzo[b]thiophen-2-yl)-4-bromo-N-(4-fluoro-3-trifluoromethyl-benzyl)benzenesulfonamide

To a solution compound 361-B (8.54 g, 20.8 mmol) in DMF (125 mL) was added KOtBu solution (23.0 mL, 1M in THF) and the reaction was stirred for 5 minutes. 18-Crown-6 (5.51 g, 20.8 mmol) and 4-(bromomethyl)-1-fluoro-2-(trifluoromethyl)-benzene (9.60 mL, 62.0 mmol) were added and the reaction was stirred for 18 h. An additional portion of KOtBu solution (10.0 mL, 1M in THF) and 18-crown-6 (2.42 g, 9.14 mmol) were added to the reaction mixture and the reaction was stirred for an additional 3 days. The reaction mixture was concentrated in vacuo and the crude material purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford compound 386 as a semi-pure material. The solid was triturated with EtOAc (10 mL), filtered, washed with an additional EtOAc (10 mL) and air-dried to afford 6.92 g of compound 386 as a white crystalline powder. ¹H-NMR (DMSO-d₆) δ: 2.38 (s, 3H), 4.97 (s, 2H), 7.41-7.50 (m, 3H), 7.66-7.70 (m, 4H), 7.92 (d, 2H), 7.94-7.98 (m, 1H), 7.98-8.03 (m, 1H); MS: m/z 586.1 (M-H)⁻.

Compound 388 4-Bromo-N-(4-fluoro-3-trifluoromethylbenzyl)-N-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)benzenesulfonamide

To a solution of compound 386 (6.89 g, 11.76 mmol) in THF (120 mL) was added MeMgCl (15.6 mL, 3M in THF) and the reaction was stirred for 18 h at ambient temperature. The crude reaction was quenched with saturated NH₄Cl solution (40 mL), the layers separated, and the organic phase washed with brine (40 mL), dried over MgSO₄, filtered and evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 6.29 g of compound 388 as a glassy yellow-orange solid. ¹H-NMR (DMSO-d₆): δ 1.34 (s, 3H), 1.62 (s, 3H), 4.61 (d, 1H), 5.11-5.04 (m, 2H), 7.37-7.30 (m, 2H), 7.45-7.38 (m, 1H), 7.54-7.45 (m, 2H), 7.83-7.78 (m, 3H), 7.91-7.86 (m, 2H), 8.41-8.35 (m, 1H); MS: m/z 584 (M-OH)⁺.

Compound 415 N-(4-Fluoro-3-trifluoromethylbenzyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

A solution of compound 388 (5.67 g, 9.41 mmol) in a 1:1 mixture of DMF and MeOH (100 mL) was treated with iPr₂NEt (3.3 mL, 18.9 mmol) and (1,1′-bis(di-tert-butylphosphino)ferrocene)palladium(II) chloride (0.311 g, 0.48 mmol) and the reaction mixture was heated at 80° C. under a pressure of 50-60 psi carbon monoxide for 18 h, cooled and the reaction mixture was concentrated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 4.33 g of compound 415 as an orange-tan glassy solid. ¹H-NMR (DMSO-d₆): δ 1.35 (s 3H), 1.63 (s, 3H), 3.94 (s, 3H), 4.66 (d, 1H), 5.14-5.06 (m, 2H), 7.55-7.29 (m, 5H), 7.83-7.76 (m, 1H), 8.02 (d, 2H), 8.19 (d, 2H), 8.41-8.33 (m, 1H); MS: m/z 564.2 (M-OH)⁺.

Compound 361 N-(4-Fluoro-3-trifluoromethylbenzyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

To a solution of compound 415 (5.33 g, 7.44 mmol) in a 5:1 THF/water mixture (100 mL) was added LiOH.H₂O (0.420 g, 10.0 mmol) and the reaction was stirred for 18 h at ambient temperature. An additional portion of LiOH.H₂O (0.084 g, 2.0 mmol) was added, the reaction was stirred for an additional 18 h, and the organics were evaporated in vacuo. The crude residue was diluted with water (100 mL), acidified with 1N HCl (12.0 mL), the precipitate filtered, washed with water and dried under vacuum to afford 4.10 g of compound 361 as a white solid. ¹H-NMR (DMSO-d₆): δ 1.36 (s, 3H), 1.63 (s, 3H), 4.66 (d, 1H), 5.15-5.04 (m, 2H), 7.55-7.29 (m, 5H), 7.84-7.76 (m, 1H), 7.99 (d, 2H), 8.16 (d, 2H), 8.42-8.34 (m, 1H), 13.63 (br s, 1H); MS: m/z 566.2 (M-H)⁻.

Compound 361, Sodium Salt

Sodium, N-(4-Fluoro-3-trifluoromethylbenzyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

To a suspension of compound 361 (4.10 g, 7.22 mmol) in water (50 mL) was added 1N NaOH (7.10 mL, 7.10 mmol) and the reaction mixture was refluxed briefly and cooled back to ambient temperature. The turbid reaction was filtered, the filtrate frozen and lyophilized to afford a fluffy product. The product was stirred with hexanes (100 mL), filtered, and the powder dried under vacuum at 50° C. to afford 4.18 g of the sodium salt of compound 361 as a cream-colored powder. ¹H-NMR (DMSO-d₆): δ 1.26 (s, 3H), 1.61 (s, 3H), 4.46 (d, 1H), 5.05 (s, 1H), 5.13 (d, 1H), 7.35-7.28 (m, 2H), 7.43-7.36 (m, 1H), 7.52-7.46 (m, 1H), 7.57-7.53 (m, 1H), 7.75 (d, 2H), 7.81-7.70 (m, 1H), 8.01 (d, 2H), 8.41-8.36 (m, 1H); MS: m/z 566.2 (M-H)⁻.

Following the procedure described above for example 70 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 730 N-(3-Acetyl-benzo[b]thiophen-2-yl)-4-bromo-N-(4-fluoro-benzyl)benzene-sulfonamide

¹H-NMR (DMSO-d₆): δ 2.30 (s, 3H), 4.86 (br s, 2H), 7.19-7.11 (m, 2H), 7.40-7.33 (m, 2H), 7.47-7.41 (m, 2H), 7.75-7.70 (m, 2H), 7.93-7.88 (m, 2H), 7.98-7.93 (m, 1H), 8.05-7.99 (m, 1H); MS: m/z 517.9 (MH⁺).

Compound 731 N-(3-Acetyl-benzo[b]thiophen-2-yl)-4-bromo-N-(4-(trifluoromethoxy)-benzyl)benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.28 (s, 3H), 4.91 (br s, 2H), 7.33 (d, 2H), 7.49-7.42 (m, 4H), 7.75-7.70 (m, 2H), 7.93-7.88 (m, 2H), 7.98-7.93 (m, 1H), 8.05-7.99 (m, 1H); MS: m/z 583.9 (MH⁺).

Compound 732 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(benzyl)-4-bromobenzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.28 (s, 3H), 4.86 (br s, 2H), 7.35-7.28 (m, 5H), 7.46-7.41 (m, 2H), 7.74-7.70 (m, 2H), 7.92-7.88 (m, 2H), 7.97-7.92 (m, 1H), 8.05-7.99 (m, 1H); MS: m/z 500.0 (MH⁺).

Compound 733 N-(3-Acetyl-benzo[b]thiophen-2-yl)-4-bromo-N-(3-chloro-4-fluoro-benzyl)benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.37 (s, 3H), 4.88 (br s, 2H), 7.41-7.33 (m, 2H), 7.48-7.43 (m, 2H), 7.53 (dd, 1H), 7.76-7.77 (m, 2H), 7.93-7.89 (m, 2H), 7.99-7.94 (m, 1H), 8.05-7.99 (m, 1H); MS: m/z 552.0 (MH⁺).

Compound 734 N-(4-Fluorobenzyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-bromo-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.17 (s, 3H), 1.63 (s, 3H), 4.34 (d, 1H), 5.11-5.02 (m, 2H), 7.22-7.04 (m, 4H), 7.38-7.27 (m, 2H), 7.84-7.76 (m, 3H), 7.90 (d, 2H), 8.44-8.36 (m, 1H); MS: m/z 516 (M-OH)⁺.

Compound 735 N-(3-(1-Hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxybenzyl)-4-bromo-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.10 (s, 3H), 1.63 (s, 3H), 4.38 (d, 1H), 5.08 (s, 1H), 5.12 (d, 1H), 7.38-7.25 (m, 6H), 7.84-7.77 (m, 3H), 7.89 (d, 2H), 8.43-8.35 (m, 1H); MS: m/z 582.0 (M-OH)⁺.

Compound 736 N-(Benzyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-bromo-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.09 (s, 3H), 1.64 (s, 3H), 4.33 (d, 1H), 5.12-5.03 (m, 2H), 7.17-7.09 (m, 2H), 7.37-7.20 (m, 5H), 7.84-7.75 (m, 3H), 7.89 (d, 2H), 8.43-8.36 (m, 1H); MS: m/z 498.0 (M-OH)⁺.

Compound 737 N-(3-Chloro-4-fluorobenzyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-bromo-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.33 (s, 3H), 1.63 (s, 3H), 4.97 (d, 1H), 5.02 (d, 1H), 5.11 (s, 1H), 7.20-7.12 (m, 1H), 7.39-7.25 (m, 4H), 7.84-7.76 (m, 3H), 7.90 (d, 2H), 8.43-8.35 (m, 1H); MS: m/z 550.0 (M-OH)⁺.

Compound 781 Sodium, N-(3-(1-Hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy)benzyl-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.06 (s, 3H), 1.63 (s, 3H), 4.27 (d, 1H), 5.05 (s, 1H), 5.13 (d, 1H), 7.35-7.22 (m, 6H), 7.75 (d, 2H), 7.81-7.77 (m, 1H), 8.01 (d, 2H), 8.43-8.39 (m, 1H); MS: m/z 564.1 (M-H)⁻.

Example 71

Compound 655 N-(Benzo[b]thiophen-2-yl)-4-bromo-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

To a solution of triphenyl phosphine (1.97 g, 7.50 mmol) in THF (50 mL) was added 40% DEAD in toluene solution (3.40 mL, 7.65 mmol) and the reaction mixture was stirred for 2 min. Compound 361-A (1.84 g, 5.00 mmol) was added, the reaction mixture stirred an additional 5 min, to which was added 5,5,5-trifluoropentan-1-ol (0.62 mL, 5.99 mmol) and the reaction mixture was stirred for 18 h. The reaction mixture was concentrated in vacuo and the crude material purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 2.19 g of compound 655 as a tan powder. ¹H-NMR (DMSO-d₆): δ 1.64-1.49 (m, 4H), 2.37-2.17 (m, 2H), 3.71-3.64 (m, 2H), 7.27 (s, 1H), 7.47-7.34 (m, 2H), 7.69-7.63 (m, 2H), 7.92-7.77 (m, 4H).

N-(3-Acetylbenzo[b]thiophen-2-yl)-4-bromo-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide (658-A)

To compound 655 (2.16 g, 4.39 mmol) was added acetic anhydride (50 mL) and 85% H₃PO₄ (0.50 mL) and the reaction was refluxed for 18 h, cooled, and the reaction mixture concentration under reduced pressure. The crude residue was partitioned between EtOAc (250 mL) and saturated NaHCO₃ (50 mL). Insoluble material was filtered, the organic layer washed with brine (50 mL), dried over MgSO₄, filtered and concentrated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 1.26 g of compound 658-A as a thick, colorless oil. ¹H-NMR (DMSO-d₆): δ 1.64-1.50 (m, 2H), 1.78-1.64 (m, 2H), 2.37-2.18 (m, 2H), 2.66 (s, 3H), 3.67 (br s, 2H), 7.53-7.42 (m, 2H), 7.67-7.60 (m, 2H), 7.90-7.83 (m, 2H), 7.99-7.92 (m, 1H), 8.17-8.10 (m, 1H); MS: m/z 534 (MH⁺).

Compound 656 4-Bromo-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

To a solution of compound 658-A (1.26 g, 2.35 mmol) in THF (25 mL) was added MeMgCl (3.95 mL, 3M in THF) and the reaction was stirred for 18 h. The reaction was quenched with a saturated NH₄Cl solution (10 mL), the organics were washed with brine (10 mL), dried with MgSO₄, filtered and evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 0.865 g of compound 656 as a colorless glass. ¹H-NMR (DMSO-d₆): δ 1.55-1.37 (m, 3H), 1.74-1.65 (m, 4H), 1.78 (s, 3H), 2.29-2.14 (m, 2H), 3.26-3.17 (m, 1H), 3.89-3.79 (m, 1H), 5.26 (s, 1H), 7.39-7.32 (m, 2H), 7.83-7.74 (m, 3H), 7.91-7.85 (m, 2H), 8.53-8.47 (m, 1H); MS: m/z 532.2 (M-OH)⁺.

N-(3-(1-Hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-carbomethoxy-benzenesulfonamide (658-B)

A solution of compound 656 (0.828 g, 1.50 mmol) in a 1:1 mixture of DMF and MeOH (50 mL) was treated with iPr₂NEt (0.53 mL, 3.04 mmol) and (1,1′-bis(di-tert-butylphosphino)ferrocene)palladium(II) chloride (0.050 g, 0.08 mmol) and the reaction mixture was heated at 80° C. under a pressure of 50-60 psi carbon monoxide for two days. The reaction mixture was cooled, concentrated in vacuo and the material was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 0.514 g of compound 658-B. ¹H-NMR (DMSO-d₆): δ 1.55-1.37 (m, 3H), 1.75-1.63 (m, 4H), 1.79 (s, 3H), 2.29-2.14 (m, 2H), 3.30-3.21 (m, 1H), 3.91-3.82 (m, 1H), 3.93 (s, 3H), 5.27 (s, 1H), 7.40-7.32 (m, 2H), 7.81-7.75 (m, 1H), 8.02-7.98 (m, 2H), 8.21-8.16 (m, 2H), 8.53-8.47 (m, 1H); MS: m/z 512.2 (M-OH)⁺.

Compound 658 Sodium, N-(3-(1-Hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-carboxy-benzenesulfonamide

To compound 658-B (0.506 g, 0.96 mmol) in a 5:1 THF/water mixture (25 mL) was added LiOH.H₂O (0.084 g, 2.00 mmol) and the reaction mixture was stirred for 18 h at ambient temperature. The solvent was evaporated in vacuo, the residue dissolved in H₂O (10 mL) and acidified with 1N HCl (2.0 mL). The precipitate was filtered, washed with H₂O, and dried under vacuum to afford the 0.460 g of the carboxylic acid of compound 658. product. Water (10 mL) was added followed by 1N NaOH (0.88 mL, 0.88 mmol), the turbid reaction filtered, and the filtrate frozen and lyophilized to afford 0.478 g of the sodium salt of compound 658 as a cream-colored powder. ¹H-NMR (DMSO-d₆): δ 1.58-1.36 (m, 3H), 1.76-1.62 (m, 4H), 1.80 (s, 3H), 2.31-2.11 (m, 2H), 3.21-3.09 (m, 1H), 3.91-3.78 (m, 1H), 5.27 (s, 1H), 7.38-7.29 (m, 2H), 7.70 (d, 2H), 7.82-7.75 (m, 1H), 8.00 (d, 2H), 8.56-8.47 (m, 1H); MS: m/z 514.2 (M-H)⁻.

Following the procedure described above for example 71 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 504 N-(3-(1-Hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.68 (s, 3H), 1.77 (s, 3H), 2.51-2.42 (m, 1H), 2.88-2.73 (m, 1H), 3.50-3.41 (m, 1H), 3.92 (s, 3H), 4.18-4.09 (m, 1H), 5.26 (s, 1H), 7.41-7.34 (m, 2H), 7.84-7.78 (m, 1H), 7.99 (d, 2H), 8.20 (d, 2H), 8.49-8.42 (m, 1H); MS: m/z 484.2 (M-OH)⁺.

Compound 505 Sodium, N-(3-(1-Hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 1.68 (s, 3H), 1.80 (s, 3H), 2.49-2.38 (m, 1H), 2.85-2.72 (m, 1H), 3.40-3.31 (m, 1H), 4.13-4.03 (m, 1H), 5.28 (s, 1H), 7.40-7.32 (m, 2H), 7.70 (d, 2H), 7.84-7.79 (m, 1H), 8.02 (d, 2H), 8.53-8.46 (m, 1H); MS: m/z 486.2 (M-H)⁻.

Compound 654 N-(Benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-bromo-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.05-0.02 (m, 2H), 0.42-0.35 (m, 2H), 0.78-0.64 (m, 1H), 1.41 (q, 2H), 3.71 (t, 2H), 7.26 (s, 1H), 7.41-7.32 (m, 2H), 7.69-7.62 (m, 2H), 7.90-7.76 (m, 4H).

Compound 657 Sodium, N-(2-Cyclopropyl-ethyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ −0.02-0.16 (m, 2H), 0.40-0.31 (m, 2H), 0.68-0.56 (m, 1H), 1.27-1.08 (m, 1H), 1.66-1.52 (m, 1H), 1.70 (s, 3H), 1.79 (s, 3H), 3.24-3.11 (m, 1H), 3.93-3.80 (m, 1H), 5.28 (s, 1H), 7.38-7.30 (m, 2H), 7.68 (d, 2H), 7.83-7.75 (m, 1H), 8.01 (d, 2H), 8.56-8.48 (m, 1H); MS: m/z 458.2 (M-H)⁻.

Example 72

Compound 503 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(butyl)-4-bromo-benzenesulfonamide

To a suspension of compound 361-B (0.600 g, 1.46 mmol) in 1-butyl-3-methyl-1H-imidazol-3-ium tetrafluoroborate (12 mL) was added powdered KOH (0.397 g, 7.08 mmol) followed by 1-bromobutane (1.00 mL, 9.27 mmol) and the reaction was heated at 150° C. for 2.5 h. Additional 1-bromobutane (0.50 mL, 4.63 mmol) was added, the reaction mixture was heated for an additional 1 h, to which was added additional KOH (0.198 g, 3.53 mmol), and the reaction mixture was heated at 150° C. for 2 days. The reaction mixture was cooled to ambient temperature, diluted with H₂O (100 mL), extracted with EtOAc (200 mL), the organic extract washed with H₂O (2×100 mL), brine (100 mL), dried over MgSO₄, filtered and concentrated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 0.347 g of compound 503 as a tan semi-solid. ¹H-NMR (DMSO-d₆): δ 0.86 (t, 3H), 1.35 (h, 2H), 1.60 (p, 2H), 2.66 (s, 3H), 3.63 (br s, 2H), 7.51-7.43 (m, 2H), 7.64-7.59 (m, 2H), 7.88-7.84 (m, 2H), 7.97-7.93 (m, 1H), 8.16-8.11 (m, 1H); MS: m/z 466.1 (MH⁺).

Compound 506 N-(Butyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-bromo-benzenesulfonamide

To a solution of compound 503 (0.330 g, 0.71 mmol) in THF (10 mL) was added MeMgCl (1.20 mL, 3M in THF) and the reaction mixture was stirred for 18 h. The reaction mixture was quenched with saturated NH₄Cl solution (5 mL), brine (5 mL), dried over MgSO₄, filtered and evaporated in vacuo. The material was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 0.22 g of compound 506 as an off-white powder. ¹H-NMR (DMSO-d₆): δ 0.82 (t, 3H), 1.42-1.15 (m, 3H), 1.67-1.53 (m, 1H), 1.71 (s, 3H), 1.79 (s, 3H), 3.21-3.12 (m, 1H), 3.84-3.74 (m, 1H), 5.28 (s, 1H), 7.38-7.32 (m, 2H), 7.77-7.73 (m, 2H), 7.82-7.77 (m, 1H), 7.90-7.85 (m, 2H), 8.54-8.49 (m, 1H); MS: m/z 464 (M-OH)⁻.

Compounds 343 and 516 N-(Butyl)-N-(3-(1-hydroxy-1-methylethyl)-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide (Cpd 343) and N-(Butyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide (Cpd 516)

To a solution of compound 506 (0.201 g, 0.42 mmol) in DMF (5 mL) and MeOH (2 mL) was added iPr₂NEt (0.15 mL, 0.86 mmol) followed by (1,1′-bis(diphenylphosphino)ferrocene)palladium(II) chloride (0.035 g, 0.04 mmol). The reaction mixture was degassed with argon, cooled on a dry-ice acetone bath and charged with carbon monoxide. The reaction vessel was sealed and heated at 60° C. for 18 h. The reaction was cooled to ambient temperature, iPr₂NEt (0.15 mL, 0.86 mmol) and (1,1′-bis(diphenylphosphino)ferrocene)palladium(II) chloride (0.035 g, 0.04 mmol) were added, the reaction mixture was cooled on a dry-ice acetone bath, charged with carbon monoxide, the reaction vessel sealed and heated at 60° C. for 7 h. This step was repeated once more and heated at 60° C. for 5 days. The reaction mixture was cooled, concentrated in vacuo, dissolved in MeOH, filtered, and the filtrate concentrated in vacuo. The crude residue was chromatographed reverse-phase (25-95% acetonitrile/water+0.1% TFA) and lyophilized to afford 0.009 g of compound 343 and 0.015 g of compound 516.

Compound 343 N-(Butyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.81 (t, 3H), 1.43-1.15 (m, 3H), 1.62-1.54 (m, 1H), 1.72 (s, 3H), 1.80 (s, 3H), 3.24-3.15 (m, 1H), 3.87-3.77 (m, 1H), 5.29 (br s, 1H), 7.39-7.32 (m, 2H), 7.80-7.75 (m, 1H), 7.95 (d, 2H), 8.17 (d, 2H), 8.55-8.48 (m, 1H), 13.58 (s, 1H); MS: m/z 446.3 (M-H)⁻.

Compound 516 N-(Butyl)-N-(3-(1-hydroxy-1-methylethyl)-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 0.81 (t, 3H), 1.43-1.15 (m, 3H), 1.67-1.53 (m, 1H), 1.71 (s, 3H), 1.80 (s, 3H), 3.24-3.15 (m, 1H), 3.87-3.77 (m, 1H), 3.92 (s, 3H), 5.28 (br s, 1H), 7.39-7.32 (m, 2H), 7.80-7.74 (m, 1H), 7.97 (d, 2H), 8.19 (d, 2H), 8.54-8.48 (m, 1H); MS: m/z 444.3 (M-OH)⁺.

Example 73

N-(Benzo[b]thiophen-2-yl)-4-cyanobenzenesulfonamide (389-A)

To a stirred solution of compound 1-C (0.927 g, 5.0 mmol) in pyridine (10 mL) and methylene chloride (5 mL), cooled on an ice bath, was added 4-cyanobenzene-1-sulfonyl chloride (1.01 g, 5.0 mmol) portion-wise over 3 min. The reaction was allowed to warm slowly to ambient temperature and allowed to stir for 72 h. The reaction mixture was concentrated under reduced pressure, the crude residue was partitioned between EtOAc (100 mL) and 1N HCl (25 mL), the layers separated, the organic phase washed with brine (25 mL), dried over MgSO₄, filtered and evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 1.22 g of compound 389-A as a tan-brown powder. ¹H-NMR (DMSO-d₆): δ 6.91 (s, 1H), 7.33-7.21 (m, 2H), 7.69-7.64 (m, 1H), 7.82-7.76 (m, 1H), 7.99-7.93 (m, 2H), 8.11-8.05 (m, 2H), 11.49 (br s, 1H); MS: m/z 313.1 (M-H)⁻.

N-(3-Acetyl-benzo[b]thiophen-2-yl)-4-cyanobenzenesulfonamide (389-B)

To a suspension of compound 389-A (1.22 g, 3.88 mmol) in DCM (10 mL), cooled in an ice bath, was added a pre-mixed (5 min) solution of ice-cold acetyl chloride (0.36 mL, 5.06 mmol) and SnCl₄ (0.51 mL, 4.32 mmol) in DCM (25 mL). The reaction mixture was allowed to warm slowly to ambient temperature and stir for 18 h. The reaction mixture was quenched with a saturated NH₄Cl solution (25 mL), filtered through a pad of celite, the organics dried over MgSO₄, filtered and concentrated under vacuum to afford 1.62 g of compound 389-B as a semi-pure product. ¹H-NMR (DMSO-d₆): δ 2.55 (s, 3H), 7.22-7.14 (m, 1H), 7.31-7.24 (m, 1H), 7.67 (d, 1H), 8.04-7.92 (m, 4H), 8.21 (d, 1H); MS: m/z 355.1 (M-H)⁻.

Compound 387 N-(3-Acetyl-benzo[b]thiophen-2-yl)-4-cyano-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

To a solution of compound 389-B (assume 3.88 mmol) in DMF (25 mL) was added a KOtBu solution (4.30 mL, 1M in THF), the reaction was stirred for 5 min, to which was added then 18-C-6 (1.03 g, 3.89 mmol) and 4-(bromomethyl)-1-fluoro-2-(trifluoromethyl)benzene (1.80 mL, 11.63 mmol). The reaction mixture was stirred for 4 days, concentrated in vacuo, and the material was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 1.59 g of compound 387 as a tan glass. ¹H-NMR (DMSO-d₆): δ 2.37 (s, 3H), 5.02 (br s, 2H), 7.52-7.42 (m, 3H), 7.74-7.66 (m, 2H), 8.05-7.92 (m, 4H), 8.22-8.16 (m, 2H).

Compound 389 4-Acetyl-N-(4-fluoro-3-trifluoromethylbenzyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-benzenesulfonamide

To a solution of compound 387 (0.267 g, 0.50 mmol) in THF (5 mL) was added MeMgCl (1.90 mL, 3M in THF), portion-wise over 5 h, and the reaction was stirred for an additional 30 min. The reaction was quenched with a saturated NH₄Cl solution (5 mL), the layers partitioned, the organic phase dried over MgSO₄, filtered and evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 0.075 g of compound 389 as a glassy yellow solid. ¹H-NMR (DMSO-d₆): δ 1.35 (s, 3H), 1.63 (s, 3H), 2.68 (s, 3H), 4.64 (d, 1H), 5.15-5.06 (m, 2H), 7.53-7.30 (m, 5H), 7.83-7.76 (m, 1H), 8.02 (d, 2H), 8.19 (d, 2H), 8.42-8.35 (m, 1H); MS: m/z 548.2 (M-OH)⁺.

Following the procedure described above for example 73 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 772 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-cyano-benzenesulfonamide

¹H-NMR (DMSO-d₆): δ 2.27 (s, 3H), 4.95 (s, 2H), 7.32-7.34 (d, 2H), 7.43-7.49 (m, 5H), 7.93-8.03 (m, 5H), 8.16-8.18 (m, 2H); MS: m/z 531.0 (MH⁺).

Compound 773 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-cyano-benzenesulfonamide

MS: m/z 481.0 (MH⁺).

Example 74

N-(3-Acetyl-benzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide (344-A)

To a suspension of compound 283-A (1.05 g, 3.01 mmol) in DCM (4 mL), in an ice bath, was added a pre-mixed (5 min) solution of acetyl chloride (0.28 mL, 3.93 mmol) and SnCl₄ (0.39 mL, 3.31 mmol) in DCM (20 mL). The reaction mixture was allowed to warm slowly to ambient temperature and stir for 18 h. The reaction mixture was quenched with a saturated NH₄Cl solution (25 mL), filtered through a pad of celite, the organics dried over MgSO₄, filtered and concentrated under vacuum. The residue was triturated with EtOAc (4 mL), filtered and air dried to afford 0.925 g of compound 344-A as a tan powder. ¹H-NMR (DMSO-d₆): δ 2.55 (s, 3H), 3.86 (s, 3H), 7.24 (t, 1H), 7.32 (t, 1H), 7.73 (d, 1H), 7.94 (d, 2H), 8.11 (d, 2H), 8.16 (d, 1H); MS: m/z 390.0 (MH⁺).

Compound 339 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(butyl)-4-carbomethoxy-benzenesulfonamide

To a solution of triphenyl phosphine (0.933 g, 3.56 mmol) in THF (30 mL) was added a 40% DEAD-toluene solution (1.60 mL, 3.60 mmol), the reaction mixture was stirred for 2 min, compound 344-A (0.924 g, 2.37 mmol) was added, the reaction mixture was stirred for an additional 5 min, to which was added n-butanol (0.26 mL, 2.84 mmol) and the reaction was stirred for 4 days. The reaction mixture was concentrated in vacuo and the crude residue purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 0.624 g of compound 339 as a white foam. ¹H-NMR (DMSO-d₆): δ 0.86 (t, 3H), 1.35 (h, 2H), 1.61 (p, 2H), 2.67 (s, 3H), 3.65 (br s, 2H), 3.91 (s, 3H), 7.52-7.43 (m, 2H), 7.87-7.83 (m, 2H), 7.94-7.91 (m, 1H), 8.18-8.11 (m, 3H); MS: m/z 446.1 (MH⁺).

Compound 342 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(butyl)-4-carboxy-benzenesulfonamide

To compound 339 (0.361 g, 0.81 mmol) in a 5:1 THF/water mixture (10 mL) was added LiOH.H₂O (0.042 g, 1.00 mmol) and the reaction mixture was stirred for 2.5 h. The solvent was evaporated in vacuo, the residue diluted with H₂O (5 mL), acidified with 1N HCl (1.0 mL), the precipitate filtered, washed with H₂O, and dried under vacuum to afford 0.334 g of compound 342 as a white powder. ¹H-NMR (DMSO-d₆): δ 0.86 (t, 3H), 1.35 (h, 2H), 1.61 (p, 2H), 2.67 (s, 3H), 3.65 (br s, 2H), 7.53-7.41 (m, 2H), 7.82 (d, 2H), 7.96-7.90 (m, 1H), 8.18-8.10 (m, 3H), 13.63 (s, 1H); MS: m/z 430.2 (M-H)⁻.

Compound 344 N-(Butyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-acetyl-benzenesulfonamide

To a solution of MeMgCl (0.37 mL, 3M in THF) in THF (2.5 mL) was added a solution of compound 342 (0.216 g, 0.50 mmol) in THF (2.5 mL), drop-wise, over was 2 min. Additional MeMgCl (0.54 mL, 3M in THF) was added in three portions over 4 h, and the reaction mixture was stirred for an additional 45 min. The reaction was quenched with a saturated NH₄Cl solution (5 mL), the organic layer were dried over MgSO₄, filtered, and concentrated in vacuo. The crude residue was purified by reverse-phase (25-95% acetonitrile/water+0.1% TFA), the product fractions combined, treated with poly(vinylpyridine), filtered, frozen and lyophilized to afford 0.047 g of compound 344 as a cream-colored powder. ¹H-NMR (DMSO-d₆): δ 0.81 (t, 3H), 1.50-1.14 (m, 3H), 1.68-1.53 (m, 1H), 1.72 (s, 3H), 1.80 (s, 3H), 2.68 (s, 3H), 3.24-3.12 (m, 1H), 3.89-3.77 (m, 1H), 5.31 (s, 1H), 7.40-7.32 (m, 2H), 7.81-7.74 (m, 1H), 7.97 (d, 2H), 8.91 (d, 2H), 8.56-8.48 (m, 1H); MS: m/z 428.2 (M—OH)⁺.

Example 75

N-(Benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoropropyl)-4-carbomethoxy-benzenesulfonamide (385-A)

To a solution of triphenyl phosphine (2.27 g, 8.64 mmol) in THF (60 mL) was added a 40% DEAD-toluene solution (3.85 mL, 8.67 mmol), the reaction mixture was stirred for 2 min, compound 283-A (2.0 g, 5.76 mmol) was added, the reaction mixture was stirred for an additional 5 min, to which was added 3,3,3-trifluoropropan-1-ol (0.61 mL, 6.90 mmol) and the reaction was stirred for 18 h. The reaction mixture was concentrated in vacuo and the crude residue purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 2.16 g of compound 385-A as a tan solid. ¹H-NMR (DMSO-d₆): δ 2.68-2.50 (m, 2H), 3.90 (s, 3H), 3.97 (t, 2H), 7.28 (s, 1H), 7.42-7.34 (m, 2H), 7.84-7.76 (m, 1H), 7.94-7.86 (m, 3H), 8.18-8.11 (m, 2H); MS: m/z 444.1 (MH⁺).

N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoropropyl)-4-carbomethoxy-benzenesulfonamide (385-B)

To compound 385-A (0.388 g, 0.87 mmol) was added acetic anhydride (10 mL) and 85% H₃PO₄ (0.10 mL), and the reaction was heated at 100° C. for three days. Additional acetic anhydride (10 mL) was added, the reaction mixture heated for an additional 4 more days. The reaction mixture was cooled, concentrated under vacuum, partitioned between EtOAc (100 mL) and saturated NaHCO₃ (50 mL), filtered, the organic layer washed with brine (50 mL), dried over MgSO₄, filtered, and concentrated in vacuo. The crude residue was purified by flash column chromatography (SiO₂) eluting with an EtOAc-heptane gradient to afford 0.197 g of compound 385-B as a colorless oil. ¹H-NMR (DMSO-d₆): δ 2.64 (s, 3H), 2.91-2.72 (m, 2H), 4.01-3.87 (m, 5H), 7.54-7.43 (m, 2H), 7.87 (d, 2H), 7.99-7.92 (m, 1H), 8.19-8.08 (m, 3H); MS: m/z 486.1 (MH⁺).

Compound 385 N-(3-Acetyl-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-carboxy-benzenesulfonamide

To compound 385-B (0.190 g, 0.39 mmol) in a 5:1 THF/water mixture (5 mL) was added LiOH.H₂O (0.021 g, 0.50 mmol) and the reaction mixture was stirred for 18 h at ambient temperature. The solvent was evaporated in vacuo, the crude residue dissolved in warm H₂O (5 mL), acidified with 1N HCl (0.5 mL), the precipitate filtered, washed with H₂O, and dried under vacuum to afford 0.166 g of compound 385 as a white powder. ¹H-NMR (DMSO-d₆): δ 2.64 (s, 3H), 2.91-2.73 (m, 2H), 4.02-3.85 (m, 2H), 7.54-7.43 (m, 2H), 7.84 (d, 2H), 7.99-7.91 (m, 1H), 8.17-8.08 (m, 3H), 13.65 (s, 1H); MS: m/z 470.1 (M-H)⁻.

Example 76

Compound 341 N-(Butyl)-N-(3-(1-hydroxy-1-methyl-ethyl)-benzo[b]thiophen-2-yl)-4-(2-1-hydroxy-1-methyl-ethyl)-benzenesulfonamide

A solution of compound 339 (0.232 g, 0.52 mmol) in THF (2.5 mL) was added to a solution of MeMgCl (0.20 mL, 3M in THF) in THF (1 mL). Additional MeMgCl (0.70 mL, 3M in THF) was added to the reaction mixture over 18 h, portion-wise, the reaction was quenched with a saturated NH₄Cl solution (5 mL), the layers separated, the organic layer dried over MgSO₄, filtered, and concentrated in vacuo. The crude residue was purified by reverse-phase (25-95% acetonitrile/water+0.1% TFA), the product fractions combined, treated with poly(vinylpyridine, filtered, frozen and lyophilized to afford 0.087 g of compound 341 as an off-white powder. ¹H-NMR (DMSO-d₆): δ 0.80 (t, 3H), 1.39-1.13 (m, 3H), 1.47 (s, 6H), 1.66-1.52 (m, 1H), 1.70 (s, 3H), 1.80 (s, 3H), 3.18-3.05 (m, 1H), 3.81-3.68 (m, 1H), 5.39-5.22 (br m, 2H), 7.39-7.31 (m, 2H), 7.82-7.70 (m, 5H), 8.57-8.49 (m, 1H); MS: m/z 444.2 (M-OH)⁺.

Example 77

tert-Butyl N-(benzo[b]thiophen-2-yl)-sulfamoylcarbamate (304-A)

To a solution of chlorosulfonyl isocyanate (0.52 mL, 5.96 mmol) in DCM (5 mL) was added t-butanol (0.57 mL, 6.00 mmol), drop-wise over 1-2 min and the reaction mixture was stirred at ambient temperature for 2 h. A suspension of compound 1-C (0.928 g, 5.00 mmol) in DCM (10 mL) was treated with pyridine (1 mL), the resulting solution cooled on an ice bath and the aforementioned reaction mixture was added drop-wise over 4 min. The reaction mixture was allowed to slowly warm to ambient temperature and stirred for 18 h. The reaction mixture was concentrated in vacuo, the residue dissolved in DCM (100 mL), washed with 1N HCl (25 mL), saturated NaHCO₃ (25 mL), brine (25 mL), the organic phase dried over MgSO₄, filtered, and evaporated under vacuum. The crude solid was triturated with DCM (10 mL), filtered, washed with DCM (2 mL) and air-dried to afford 0.602 g of compound 304-A as an off-white powder. ¹H-NMR (DMSO-d₆): δ 1.39 (s, 9H), 6.98 (s, 1H), 7.37-7.24 (m, 2H), 7.72 (d, 1H), 7.84 (d, 1H), 11.11 (s, 1H), 11.40 (s, 1H); MS: m/z 351.1 (MNa⁺).

Compound 304 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-sulfamide

To a solution of Ph₃P (0.492 g, 1.88 mmol) in THF (15 mL) was added a 40% DEAD-toluene solution (0.84 mL, 1.89 mmol), the reaction mixture was stirred for 2 min, compound 304-A (0.352 g, 1.07 mmol) was added, and the reaction mixture was then split equally into 5-portions. 3,3,3-Trifluoro-propan-1-ol (0.025 mL, 0.30 mmol) was added to one-portion of the aforementioned reaction mixture, the reaction stirred for 18 h, and the solvent evaporated in vacuo. The crude residue dissolved 1:1 dichloroethane/acetic acid (2 mL), NBS (0.053 g, 0.30 mmol) was added, and the reaction mixture was stirred for 1 h. Additional NBS (0.011 g, 0.06 mmol) was added, the reaction mixture was stirred for 30 min, trifluoroacetic acid (0.50 mL) was added, and the reaction mixture was stirred for 3 days. The solvent was evaporated in vacuo, the crude residue purified by reverse-phase (25-95% acetonitrile/water+0.1% TFA), and the product fractions frozen and lyophilized to afford 0.012 g of compound 304. ¹H-NMR (DMSO-d₆): δ 2.64-2.54 (m, 2H), 3.80 (t, 2H), 7.58-7.50 (m, 2H), 7.67 (s, 2H), 7.82-7.76 (m, 1H), 8.05-8.00 (m, 1H); MS: m/z 403 (MH⁺).

Following the procedure described above for example 77 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 303 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(cyclopropylmethyl)-sulfamide

MS: m/z 361.0 (MH⁺).

Compound 849 N-(3-Bromo-benzo[b]thiophen-2-yl)-N′,N′-bis-butyl-sulfamide

MS: m/z 419.1 (MH⁺)

Example 78

Compound 850 N-Benzo[b]thiophen-2-yl-N,N′-bis-butyl-sulfamide

To a solution of Ph₃P (0.100 g, 1.88 mmol) in THF (3 mL) was added a 40% DEAD-toluene solution (0.17 mL, 0.38 mmol), the reaction mixture was stirred for 2 min, compound 304-A (0.083 g, 1.07 mmol) was added, the reaction mixture stirred for 5 min, the butan-1-ol (0.027 mL, 0.29 mmol) was added, and the reaction mixture stirred for 18 h. Trifluoroacetic acid (0.50 mL) was added, the reaction mixture stirred for 1 h, and the solvent evaporated under reduced pressure. DCM (2 mL) and TFA (1 mL) were added to the residue, the reaction mixture stirred for 3 days, the solvent evaporated in vacuo, the crude residue purified by reverse-phase chromatography (25-95% acetonitrile/water+0.1% TFA), and the product fractions frozen and lyophilized to afford 0.02 g of compound 850. ¹H-NMR (DMSO-d₆): δ 0.89-0.80 (m, 6H), 1.36-1.22 (m, 4H), 1.44-1.36 (m, 2H), 1.54-1.44 (m, 2H), 2.92 (q, 2H), 3.60 (t, 2H), 7.27 (s, 1H), 7.39-7.30 (m, 2H), 7.71 (t, 1H), 7.80-7.76 (m, 1H), 7.89-7.85 (m, 1H); MS: m/z 341.2 (MH⁺).

Example 79

N-(3-Chloro-thieno[2,3-b]pyridin-2-yl)-benzenesulfonamide (813-A)

To compound 147-F (0.26 g, 0.643 mmol) in DMF (1 mL) under argon at ambient temperature was added N-chlorosuccinimide (94.4 mg, 0.707 mmol) and the reaction mixture was stirred for 16 h. Ethyl acetate was added, the mixture washed with H₂O (2×), brine, evaporated under reduced pressure and purified by reverse phase pHPLC (C18) to afford 0.072 g of compound 813-A as a tan solid. ¹H-NMR (DMSO-d₆): δ 7.50 (dd, 1H), 7.56-7.65 (m, 2H), 7.65-7.74 (m, 1H), 7.81-7.89 (m, 2H), 8.00 (dd, 1H), 8.58 (dd, 1H).

Compound 813 N-(3-Chloro-thieno[2,3-b]pyridin-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

To a solution of compound 813-A (72.1 mg, 0.222 mmol) in DMF (1 mL) under argon was added 60% NaH (9.3 mg, 0.233 mmol) and the reaction mixture was stirred for 15 min at ambient temperature. 4-Fluoro-3-trifluoromethylbenzyl bromide (0.034 mL, 0.222 mmol) was added and the reaction mixture was stirred for six days at ambient temperature. Saturated NaHCO₃ was added, the solution was extracted with EtOAc, washed with brine, dried over K₂CO₃, filtered, and evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂) eluting with CH₂Cl₂, the pure fractions combined, excess 1M ethereal hydrogen chloride added, and the mixture evaporated under reduced pressure to afford 80 mg of compound 813 as a white solid. ¹H-NMR (DMSO-d₆): δ 4.93 (s, 2H), 7.40-7.51 (m, 1H), 7.58 (dd, 1H), 7.63-7.78 (m, 4H), 7.80-7.90 (m, 1H), 7.95 (d, 2H), 8.15 (d, 1H), 8.65-8.76 (m, 1H); MS: m/z 501.04 (MH⁺).

Example 80

3-(Chloro-thieno[2,3-b]pyridin-2-yl)-amine (814-A)

To a homogeneous solution of compound 147-E (0.30 g, 1.34 mmol) in DMF (4 mL) under argon at ambient temperature was added N-chlorosuccinimide (0.22 g, 1.65 mmol), the reaction mixture was stirred for seven days, EtOAc was added, and the precipitate filtered to afford 0.12 g of compound 814-A as a white solid MS: m/z 185 (MH⁺).

3-(Chloro-thieno[2,3-b]pyridin-2-yl)-3-carbomethoxy-benzenesulfonamide (814-B)

To a solution of compound 814-A (0.17 g, 0.654 mmol) in pyridine (1.7 mL) under argon at ambient temperature was added 3-chlorosulfonyl-benzoic acid methyl ester (0.153 g, 0.654 mmol) and the reaction mixture was stirred at ambient temperature for 24 h. An additional portion of 3-chlorosulfonyl-benzoic acid methyl ester (0.03 g, 0.128 mmol) was added and the reaction mixture was stirred for an additional 48 h, at which time another portion of 3-chlorosulfonyl-benzoic acid methyl ester (0.043 g, 0.183 mmol) was added and the reaction mixture was allowed to stir for 18 h. The solvent was evaporated under reduced pressure and the crude residue purified by flash column chromatography (SiO₂) eluting with 1:1 heptane:CH₂Cl₂, CH₂Cl₂, and 1:3 acetone:CH₂Cl₂ to afford 0.12 g of compound 814-B. MS: m/z 383.05 (MH⁺).

Compound 816 N-(3-Chloro-thieno[2,3-b]pyridin-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carbomethoxy-benzenesulfonamide

To a solution of Compound 814-B (0.12 g, 0.313 mmol) in DMF (2 mL) under argon was added 60% NaH (13.8 mg, 0.345 mmol) and the reaction mixture was stirred at ambient temperature for 15 min. 4-Fluoro-3-trifluoromethylbenzyl bromide (0.048 mL, 0.329 mmol) was added, the reaction mixture stirred for five days, water added, the solution extracted with EtOAc, washed with brine, dried with K₂CO₃, filtered, evaporated under reduced pressure, and purified by reverse phase pHPLC (C₁₈) to afford 0.06 g of compound 816 as a clear oil. MS: m/z 559.0 (MH⁺).

Compound 814 N-(3-Chloro-thieno[2,3-b]pyridin-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-3-carboxy-benzenesulfonamide

To a solution of compound 816 (0.055 g, 0.0983 mmol) in methanol (5.5 mL) was added 3N NaOH (0.066 ml, 0.197 mmol) and the reaction mixture was stirred at ambient temperature for six days, the solvent evaporated under reduced pressure, the residue dissolved in 0.1% TFA in acetonitrile/DMSO, and purified by reverse phase pHPLC (C₁₈) to afford 0.04 g of compound 814 as a white solid. MS: m/z 545.07 (MH⁺).

Example 81

Compound 815-A was prepared by the method used to synthesize compound 814-B in Example 80, steps A and B.

N-(3-Chloro-thieno[2,3-b]pyridin-2-yl)-N-(3,3,3-trifluoro-propyl)-4-carbomethoxy-benzenesulfonamide (815-B)

To a flask under argon was added Ph₃P (0.268 g, 0.101 mmol), THF (7 mL), and 40% DEAD in toluene (0.449 mL, 0.101 mmol) and the reaction mixture was stirred for 2 min. Compound 815-A (0.258 g, 0.674 mmol) was added, the reaction mixture stirred for five min, to which was added 3,3,3-trifluoro-propan-1-ol (0.095 g, 0.809 mmol) in THF (3 mL) and the reaction mixture stirred at ambient temperature for six days. The solvent was evaporated under reduced pressure and the residue purified by reverse phase pHPLC (C₁₈) to afford 0.167 g of compound 815-B. MS: m/z 479.1 (MH⁺).

Compound 815 N-(3-Chloro-thieno[2,3-b]pyridin-2-yl)-N-(3,3,3-trifluoro-propyl)-4-carboxy-benzenesulfonamide

To a solution of compound 815-B (0.167 g, 0.348 mmol) in methanol (12 mL), under argon, was added 3N NaOH (0.116 mL, 0.348 mmol) and the reaction mixture was stirred at ambient temperature 18 h. An additional portion of 3N NaOH (0.116 mL, 0.348 mmol) was added and the reaction mixture was stirred for six days. 1N HCl (0.804 mL, 0.804 mmol) was added to the reaction and the precipitate filtered to afford 0.115 g of compound 815 as a white solid. MS: m/z 465.0 (MH⁺).

Example 82

Compound 499 4-Amino-N-(benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

A Paar flask containing 5% sulfided Pd/C (0.05 g, 10% w/w), compound 498 (0.49 g, 1.14 mmol) and methanol (20 mL) was reacted under hydrogen atmosphere for 3 days. The catalyst was filtered through a pad of celite and the filtrate evaporated under reduced pressure to afford 0.49 g of compound 499 as an off-white greenish solid. ¹H-NMR (CDCl₃): δ 2.48 (m, 2H), 3.78-3.87 (m, 2H), 6.63 (d, 2H), 7.14 (s, 1H), 7.30-7.40 (m, 2H), 7.48 (d, 2H), 7.65-7.75 (m, 2H); MS: m/z 401.19 (MH⁺).

Compound 585 4-Amino-N-(3-chloro-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

To a solution of compound 499 (0.18 g, 0.450 mmol) in DMF (2.5 mL) was added N-chlorosuccinimide (0.084 g, 0.494 mmol) and the reaction mixture stirred at ambient temperature for 3 days. Ether was added to the reaction mixture, the organics washed with H₂O, brine, and the solvent evaporated under reduced pressure. The crude residue was purified by reverse phase pHPLC (C₁₈) to afford 0.036 g of compound 585 as an amber gum. ¹H-NMR (CDCl₃): δ 2.42-2.60 (m, 2H), 3.81-3.87 (m, 2H), 6.65-6.72 (m, 2H), 7.42-7.50 (m, 2H), 7.57-7.63 (m, 2H), 7.69-7.75 (m, 1H), 7.77-7.84 (m, 1H); MS: m/z 435.14 (MH⁺).

Following the procedure described above for example 82 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 586 4-Amino-N-(benzo[b]thiophen-2-yl)-3-chloro-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.40-2.58 (m, 2H), 3.79-3.88 (m, 2H), 6.73 (d, 1H), 7.17 (s, 1H), 7.30-7.43 (m, 3H), 7.65 (d, 1H), 7.68-7.76 (m, 2H); MS: m/z 435.14 (MH⁺).

Compound 587 4-Amino-N-(3-bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

Compound 587 was prepared using the methodology in Example 82, step B, substituting NBS for NCS. ¹H-NMR (CDCl₃): δ 2.43-2.61 (m, 2H), 3.80-3.89 (m, 2H), 6.65-6.73 (m, 2H), 7.42-7.50 (m, 2H), 7.58-7.65 (m, 2H), 7.70-7.76 (m, 1H), 7.77-7.83 (m, 1H); MS: m/z 479.23 (MH⁺).

Compound 588 4-Amino-3-bromo-N-(3-bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

Compound 588 was isolated as a by-product from the synthesis of compound 587, prepared by using the methodology in Example 82, step B, substituting NBS for NCS. ¹H-NMR (CDCl₃): δ 2.44-2.62 (m, 2H), 3.82-3.90 (m, 2H), 6.76 (d, 1H), 7.44-7.51 (m, 2H), 7.54 (dd, 1H), 7.72-7.77 (m, 1H), 7.78-7.84 (m, 1H), 7.91 (d, 1H); MS: m/z 558.92 (MH⁺).

Compound 650 4-Amino-N-(3-bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

Compound 650 was prepared using the methodology in Example 1, steps C and D, and Example 82, steps A and B. ¹H-NMR (CDCl₃): δ 4.78 (s, 2H), 6.65-6.74 (m, 2H), 7.01-7.10 (m, 1H), 7.36-7.44 (m, 2H), 7.45-7.56 (m, 2H), 7.59-7.69 (m, 3H), 7.70-7.74 (m, 1H); MS: m/z 559.08 (MH⁺).

Compound 651 4-Amino-3-bromo-N-(3-bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

Compound 651 was isolated as a by-product from the synthesis of compound 650, prepared by using the methodology in Example 82, step B, substituting NBS for NCS. ¹H-NMR (CDCl₃): δ 4.79 (s, 2H), 6.77 (d, 1H), 7.07 (t, 1H), 7.37-7.58 (m, 5H), 7.64-7.76 (m, 2H), 7.92 (d, 1H); MS: m/z 638.85 (MH⁺).

Compound 653 4-Amino-N-(benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-benzenesulfonamide

Compound 653 was prepared using the methodology in Example 1, steps C and D, and Example 82, step A

¹H-NMR (CDCl₃): δ 4.76 (s, 2H), 6.62-6.70 (m, 2H), 7.02 (s, 1H), 7.05-7.14 (m, 1H), 7.27-7.35 (m, 2H), 7.49-7.58 (m, 4H), 7.63 (td, 2H); MS: m/z 481.2 (MH⁺).

Compound 666 4-Amino-N-(3-chloro-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

Compound 666 was prepared using the methodology in Example 1, step C, Example 3, step A, and Example 82, steps A and B. ¹H-NMR (CDCl₃): δ 1.52-1.75 (m, 4H), 1.96-2.15 (m, 2H), 3.61 (t, 2H), 6.64-6.71 (m, 2H), 7.40-7.49 (m, 2H), 7.55-7.63 (m, 2H), 7.66-7.74 (m, 1H), 7.76-7.84 (m, 1H); MS: m/z 463.11 (MH⁺).

Compound 667 4-Amino-3-chloro-N-(3-chloro-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

Compound 667 was isolated as a by-product from the synthesis of compound 585, prepared by using the methodology in Example 82, step B. MS: m/z 497.02 (MH⁺).

Compound 668 4-Amino-N-(3-bromo-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

Compound 668 was prepared using the methodology in Example 1, step C, Example 3, step A, and Example 82, steps A and B, substituting N-bromosuccinimide for N-chlorosuccinimide. ¹H-NMR (CDCl₃): δ 1.52-1.75 (m, 4H), 1.96-2.14 (m, 2H), 3.62 (t, 2H), 6.64-6.73 (m, 2H), 7.39-7.49 (m, 2H), 7.56-7.64 (m, 2H), 7.68-7.74 (m, 1H), 7.80 (dd, 1H); MS: m/z 508.90 (MH⁺).

Example 83

Compound 689-A was prepared by the method in Example 1, step C, and Example 3, step A.

Compound 688 and Compound 689 N-(Benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-methylamino-benzenesulfonamide (Cpd 688) and N-(benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-dimethylamino-benzenesulfonamide (Cpd 689)

A Paar flask containing 10% Pd/C (0.15 g, 24% w/w), and compound 689-A (0.62 g, 1.54 mmol) in methanol (100 mL), contaminated with some formaldehyde, was reacted under hydrogen atmosphere for two days. The catalyst was filtered through a pad of celite and the filtrate evaporated under reduced pressure to afford 0.42 g of a mixture of compound 688 and compound 689. The crude mixture was purified by reverse phase pHPLC (C18) to afford 0.016 g of compound 688 as a white solid and 0.028 g of compound 689 as an off-white solid.

Compound 688 N-(Benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-methylamino-benzenesulfonamide

MS: m/z 387 (MH⁺).

Compound 689 N-(Benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-dimethylamino-benzenesulfonamide

MS: m/z 401 (MH⁺).

Following the procedure described above for example 83 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 690 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-methylamino-benzenesulfonamide

Compound 690 was prepared using the methodology in Example 82, step B. ¹H-NMR (CDCl₃): δ −0.04-0.00 (m, 6H), 0.34-0.46 (m, 7H), 0.61-0.76 (m, 3H), 1.43 (q, 7H), 2.94 (s, 3H), 3.6-3.72 (m, 2H), 6.71 (d, 2H), 7.38-7.49 (m, 2H), 7.63-7.74 (m, 3H), 7.75-7.83 (m, 1H); MS: m/z 421.1 (MH⁺).

Compound 691 3-Chloro-N-(3-chloro-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-methylamino-benzenesulfonamide

Compound 691 was isolated as a by-product during the synthesis of compound 690, prepared by using the methodology in Example 82, step B. ¹H-NMR (CDCl₃): δ 0.00-0.05 (m, 6H), 0.36-0.45 (m, 8H), 0.63-0.77 (m, 4H), 1.38-1.49 (m, 8H), 2.98 (s, 3H), 3.62-3.72 (m, 2H), 6.63 (d, 1H), 7.38-7.50 (m, 2H), 7.61 (dd, 1H), 7.76-7.84 (m, 1H); MS: m/z 455.09 (MH⁺).

Compound 692 3-Bromo-N-(3-bromo-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-methylamino-benzenesulfonamide

Compound 692 was isolated as a by-product during the synthesis of compound 693, prepared by using the methodology in Example 82, step B, substituting NBS for NCS. ¹H-NMR (CDCl₃): δ 0.00-0.04 (m, 6H), 0.37-0.45 (m, 7H), 0.61-0.78 (m, 3H), 1.38-1.51 (m, 8H), 2.98 (s, 3H), 3.63-3.73 (m, 2H), 6.60 (d, 1H), 7.38-7.49 (m, 2H), 7.65 (dd, 1H), 7.71 (dd, 1H), 7.76-7.84 (m, 1H), 7.91 (d, 1H); MS: m/z 544.97 (MH⁺).

Compound 693 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-methylamino-benzenesulfonamide

Compound 693 was prepared using the methodology in Example 82, step B, substituting NBS for NCS. ¹H-NMR (CDCl₃): δ −0.05-0.02 (m, 9H), 0.34-0.46 (m, 2H), 0.61-0.75 (m, 1H), 1.37-1.52 (m, 2H), 2.96 (s, 3H), 3.63-3.73 (m, 2H), 6.83 (d, 2H), 7.38-7.48 (m, 2H), 7.65-7.74 (m, 3H), 7.75-7.82 (m, 1H); MS: m/z 465.07 (MH⁺).

Example 84

Compound 507 N-(Benzo[b]thiophen-2-yl)-4-methanesulfonylamino-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

To a flask under argon was added compound 499 (52.1 mg, 0.013 mmol), THF (3 mL), DIEA (0.027 mL, 0.016 mmol) and methanesulfonyl chloride (0.010 mL, 0.013 mmol). The reaction mixture was heated at 70° C. for seven days, the solvent evaporated under reduced pressure and the crude residue purified by flash column chromatography (SiO₂) eluting with DCM, followed by reverse phase pHPLC (C₁₈) to afford 7.2 mg of compound 507 as a yellow solid. MS: m/z 479.1 (MH⁺).

Compound 676 N-(3-Chloro-benzo[b]thiophen-2-yl)-4-methanesulfonylamino-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

To N-chlorosuccinimide (55.2 mg, 0.414 mmol) under argon was added compound 507 (0.22 g, 0.460 mmol) in DMF (5 mL). The reaction mixture was stirred at ambient temperature for 18 h, another portion of N-chlorosuccinimide (55.2 mg, 0.414 mmol) was added and the reaction mixture was stirred for an additional 18 h. Ethyl acetate was added to the reaction mixture, the organics washed with water (2×), the solvent evaporated under reduced pressure and the crude residue purified by reverse phase pHPLC (C₁₈) to afford 119 mg of compound 676 as a white solid. ¹H-NMR (CDCl₃): δ 2.45-2.62 (m, 2H), 3.13 (s, 3H), 3.85-3.93 (m, 2H), 6.93 (s, 1H), 7.28-7.34 (m, 2H), 7.45-7.53 (m, 2H), 7.72-7.86 (m, 4H); MS: m/z 512.96 (MH⁺).

Following the procedure described above for example 84 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 652 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methanesulfonylamino-benzenesulfonamide

Compound 652 was prepared using the methodology in Example 1, steps C and D, and Example 82, step A, and Example 84, step A. MS: m/z 559.07 (MH⁺).

Compound 659 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methanesulfonylamino-benzenesulfonamide

Compound 659 was prepared from compound 652 using the methodology in Example 1, steps C and D, Example 82, step A, and Example 84, steps A and B. ¹H-NMR (CDCl₃): δ 3.14 (s, 3H), 4.83 (s, 2H), 6.96 (s, 1H), 7.09 (t, 1H), 7.28-7.36 (m, 2H), 7.39-7.47 (m, 2H), 7.47-7.57 (m, 2H), 7.64-7.76 (m, 2H), 7.83 (d, 2H); MS: m/z 593.05 (MH⁺).

Compound 660 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methanesulfonylamino-benzenesulfonamide

Compound 660 was prepared from compound 652 using the methodology in Example 1, steps C and D, Example 82, step A, and Example 84, steps A and B, substituting NBS for NCS. ¹H-NMR (CDCl₃): δ 3.14 (s, 3H), 4.84 (s, 2H), 7.01-7.14 (m, 2H), 7.28-7.36 (m, 2H), 7.38-7.58 (m, 4H), 7.62-7.77 (m, 2H); MS: m/z 639.08 (MH⁺).

Compound 661 3-Bromo-N-(3-bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methanesulfonylamino-benzenesulfonamide

Compound 661 was isolated as a by-product during the synthesis of compound 660

¹H-NMR (CDCl₃): δ 3.14 (s, 3H), 4.86 (s, 2H), 7.10 (t, 1H), 7.19 (s, 1H), 7.45 (dd, 2H), 7.47-7.57 (m, 2H), 7.71 (ddd, 2H), 7.78-7.81 (m, 2H), 7.78-7.81 (m, 2H), 8.05 (s, 1H).

Compound 677 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(3,3,3-trifluoro-propyl)-4-methanesulfonylamino-benzenesulfonamide

Compound 677 was prepared from compound 507 using the methodology in Example 1, steps C and D, Example 3, step A, Example 82, step A, and Example 84, steps A and B, substituting NBS for NCS. ¹H-NMR (CDCl₃): δ 2.42-2.63 (m, 2H), 3.11-3.44 (m, 3H), 3.84-3.94 (m, 2H), 6.88-0.24 (m, 1H), 7.30 (d, 1H), 7.36-7.44 (m, 1H), 7.45-7.52 (m, 1H), 7.64-7.97 (m, 4H); MS: m/z 558.93 (MH⁺).

Compound 678 N-(Benzo[b]thiophen-2-yl)-4-methanesulfonylamino-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 1.65-1.73 (m, 4H), 1.99-2.18 (m, 2H), 3.11 (s, 3H), 3.57-3.68 (m, 2H), 6.87 (s, 1H), 7.20 (d, 2H), 7.31-7.42 (m, 2H), 7.64-7.76 (m, 4H); MS: m/z 507.02 (MH⁺).

Compound 679 N-(3-Chloro-benzo[b]thiophen-2-yl)-4-methanesulfonylamino-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

MS: m/z 541.02 (MH⁺).

Compound 680 N-(3-Bromo-benzo[b]thiophen-2-yl)-4-methanesulfonylamino-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

Compound 680 was prepared using the methodology in Example 84, steps A and B, substituting N-bromosuccinimide for N-chlorosuccinimide. MS: m/z 586.93 (MH⁺).

Compound 681 3,5-Dichloro-N-(3-chloro-benzo[b]thiophen-2-yl)-4-methanesulfonylamino-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

Compound 681 was isolated as a by-product during the synthesis of compound 676 using the methodology in Example 1, steps C and D, Example 82, step A, and Example 84, steps A and B. MS: m/z 580.84 (MH⁺).

Compound 682 3,5-Dichloro-N-(3-chloro-benzo[b]thiophen-2-yl)-4-methanesulfonylamino-N-(5,5,5-trifluoro-pentyl)-benzenesulfonamide

Compound 682 was isolated as a by-product during the synthesis of compound 679 using the methodology in Example 1, steps C and D, Example 82, step A, and Example 84, steps A and B. MS: m/z 610.79 (MH⁺).

Compound 683 3-Bromo-N-(3-bromo-benzo[b]thiophen-2-yl)-4-methanesulfonylamino-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

Compound 683 was isolated as a by-product during the synthesis of compound 677 using the methodology in Example 1, steps C and D, Example 82, step A, and Example 84, steps A and B. ¹H-NMR (CDCl₃): δ 2.47-2.65 (m, 2H), 3.11-3.45 (m, 3H), 3.87-3.96 (m, 2H), 7.18 (s, 1H), 7.46-7.54 (m, 2H), 7.73-7.84 (m, 4H), 8.04-8.09 (m, 1H).

Compound 713 N-(Benzo[b]thiophen-2-yl)-3-methanesulfonylamino-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

MS: m/z 479.00 (MH⁺).

Compound 714 N-(3-Chloro-benzo[b]thiophen-2-yl)-3-methanesulfonylamino-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

¹H-NMR (CDCl₃): δ 2.45-2.62 (m, 2H), 2.96 (s, 3H), 3.88-3.98 (m, 2H), 6.76 (s, 1H), 7.44-7.52 (m, 2H), 7.53-7.63 (m, 3H), 7.63-7.69 (m, 1H), 7.71-7.81 (m, 2H); MS: m/z 512.99 (MH⁺).

Compound 715 N-(3-Bromo-benzo[b]thiophen-2-yl)-3-methanesulfonylamino-N-(3,3,3-trifluoro-propyl)-benzenesulfonamide

Compound 715 was prepared using the methodology in Example 84, steps A and B, substituting NBS for NCS. ¹H-NMR (300 MHz, CDCl₃): δ 2.46-2.64 (m, 9H), 2.96 (s, 3H), 3.90-3.99 (m, 2H), 6.70 (s, 1H), 7.45-7.53 (m, 2H), 7.64-7.70 (m, 1H), 7.71-7.81 (m, 2H); MS: m/z 558.85 (MH⁺).

Compound 716 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-methanesulfonylamino-benzenesulfonamide

¹H-NMR (CDCl₃): δ 0.00-0.06 (m, 8H), 0.37-0.47 (m, 8H), 0.61-0.77 (m, 4H), 1.40-1.52 (m, 8H), 3.12 (s, 3H), 3.67-3.76 (m, 6H), 6.97 (s, 3H), 7.27-7.33 (m, 7H), 7.41-7.51 (m, 6H), 7.68-7.88 (m, 12H); MS: m/z 485.04 (MH⁺).

Compound 717 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-methanesulfonylamino-benzenesulfonamide

Compound 717 was prepared from compound 716 using the methodology in Example 84, steps A and B, substituting NBS for NCS. ¹H-NMR (CDCl₃): δ 0.01-0.07 (m, 7H), 0.37-0.47 (m, 7H), 0.69 (t, 4H), 1.41-1.54 (m, 7H), 3.12 (s, 3H), 3.68-3.78 (m, 2H), 6.84 (s, 1H), 7.29 (d, 2H), 7.41-7.49 (m, 2H), 7.69-7.87 (m, 4H); MS: m/z 528.89 (MH⁺).

Compound 718 N-(3-Chloro-benzo[b]thiophen-2-yl)-4-cyclopropanesulfonylamino-N-(2-cyclopropyl-ethyl)-benzenesulfonamide

MS: m/z 511.02 (MH⁺).

Compound 719 N-(3-Bromo-benzo[b]thiophen-2-yl)-4-cyclopropanesulfonylamino-N-(2-cyclopropyl-ethyl)-benzenesulfonamide

Compound 719 was prepared using the methodology in Example 84, steps A and B, substituting NBS for NCS. ¹H-NMR (CDCl₃): δ 0.01-0.06 (m, 6H), 0.38-0.46 (m, 2H), 0.69 (s, 1H), 1.00-1.10 (m, 2H), 1.21-1.31 (m, 2H), 1.42-1.52 (m, 2H), 2.51-2.63 (m, 1H), 3.68-3.80 (m, 2H), 6.75 (s, 1H), 7.29-7.37 (m, 2H), 7.40-7.50 (m, 2H), 7.68-7.86 (m, 4H); MS: m/z 555.02 (MH⁺).

Compound 743 N-(Benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methanesulfonylamino-2-methoxy-benzenesulfonamide

Compound 743 was prepared using the methodology in Example 1, steps C and D, Example 82, step A, and Example 84, step A. MS: m/z 589.03 (MH⁺).

Compound 744 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methanesulfonylamino-2-methoxy-benzenesulfonamide

Compound 744 was prepared from compound 743 using the methodology in Example 84, step B. MS: m/z 622.90 (MH⁺).

Compound 766 5-Chloro-N-(3-chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-methanesulfonylamino-2-methoxy-benzenesulfonamide

Compound 766 was isolated as a by-product during the synthesis of compound 744. ¹H-NMR (CDCl₃): δ 3.10 (s, 3H), 4.07 (s, 3H), 5.07 (s, 2H), 7.05 (s, 1H), 7.11 (t, 1H), 7.41 (dd, 2H), 7.47 (s, 1H), 7.53 (dd, 2H), 7.60-7.73 (m, 2H), 7.84 (s, 1H); MS: m/z 657.0 (MH⁺).

Example 85

Compound 777 N-(2-Cyclopropyl-ethyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-(4-methyl-piperazine-1-carbonyl)-benzenesulfonamide

To a solution of compound 400 (0.100 g, 0.241 mmol) in DMF (1.5 mL) was added DIEA (0.0838 mL, 0.481 mmol), 1-methyl-piperazine (0.027 mL, 0.241 mmol) and HATU (0.110 g, 0.289 mmol) and the reaction mixture stirred at ambient temperature for 18 h. Ethyl acetate was added and the organics washed with water, brine, and evaporated under reduced pressure. The crude residue was purified by reverse phase pHPLC (C₁₈) to afford 0.108 g of compound 777 as a white solid. MS: m/z 498.18 (MH⁺).

Following the procedure described above for example 85 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 782 (S)-4-[(2-Cyclopropyl-ethyl)-(3-methyl-benzo[b]thiophen-2-yl)-sulfamoyl]-N-pyrrolidin-3-yl-benzamide

MS: m/z 484.16 (MH⁺).

Compound 783 (R)-4-[(2-Cyclopropyl-ethyl)-(3-methyl-benzo[b]thiophen-2-yl)-sulfamoyl]-N-pyrrolidin-3-yl-benzamide

MS: m/z 484.16 (MH⁺).

Example 86

Compound 803 N-(3-Isopropenyl-benzo[b]thiophen-2-yl)-N-(2,4,5-trifluoro-3-methoxy-benzyl)-ethanesulfonamide

Compound 802 was purified by reverse phase pHPLC (C₁₈) eluting with 0.1% TFA in CH₃CN/H₂O. The pure fractions were lyophilized affording complete conversion of compound 802 to compound 803 as a white solid. ¹H-NMR (CDCl₃): δ 1.48 (t, 3H), 2.04 (s, 3H), 3.30 (q, 2H), 3.95 (s, 3H), 4.84 (s, 2H), 4.94 (s, 1H), 5.40 (s, 1H), 6.94 (ddd, 1H), 7.31-7.42 (m, 2H), 7.61-7.74 (m, 2H); MS: m/z 456.01 (MH⁺).

Following the procedure described above for example 86 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 768 N-(4-Chloro-2-fluoro-5-methoxy-benzyl)-N-(3-isopropenyl-benzo[b]thiophen-2-yl)-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.48 (t, 3H), 2.02 (s, 3H), 3.29 (q, 2H), 3.73 (s, 3H), 4.86 (s, 2H), 4.93 (s, 1H), 5.38 (d, 1H), 6.95 (d, 1H), 7.04 (d, 1H), 7.31-7.40 (m, 2H), 7.61-7.73 (m, 2H); MS: m/z 454.12 (MH⁺).

Example 87

Compound 695 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-trifluoroacetamido-benzenesulfonamide

To a solution of compound 650 (0.074 g, 0.136 mmol) in pyridine (1 mL), under argon, was added methanesulfonyl chloride (0.053 mL, 0.680 mmol) and the reaction mixture was stirred at ambient temperature for 18 h. The solvent was evaporated under reduced pressure and the crude residue purified by reverse phase pHPLC (C₁₈) to afford 0.029 g of compound 695 as a white solid. ¹H-NMR (CDCl₃): δ 4.85 (s, 2H), 7.04-7.14 (m, 1H), 7.38-7.57 (m, 4H), 7.63-7.74 (m, 2H), 7.76-7.82 (m, 2H), 7.85-7.93 (m, 2H), 8.12 (s, 1H); MS: m/z 654.9 (MH⁺).

Compound 694 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(2-cyclopropyl-ethyl)-4-trifluoroacetamido-benzenesulfonamide

MS: m/z 503.05 (MH⁺).

Example 88

Compound 832 N-(3-Fluoro-propyl)-N-(3-methoxymethyl-benzo[b]thiophen-2-yl)-benzenesulfonamide

To a solution of compound 820 (38 mg, 0.10 mmol) in THF (3 mL), was added sodium hydride (16 mg, 0.40 mmol) followed by iodomethane (28 mg, 0.20) at room temperature and the reaction mixture was stirred for 2 h. The reaction mixture was quenched with water, extracted with EtOAc, the layers separated, and the organic phase dried over Na₂SO₄, filtered, and the solvent evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂) eluting with 15% ethyl acetate in hexanes, to afford 36 mg of compound 832. MS: m/z 416.2 (MNa⁺).

Following the procedure described above for Example 88 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 822 N-(3-Fluoro-propyl)-N-[3-(1-methoxy-ethyl)-benzo[b]thiophen-2-yl]-benzenesulfonamide

MS: m/z 430.0 (MNa⁺).

Compound 839 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-[3-(1-methoxy-ethyl)-benzo[b]thiophen-2-yl]-ethanesulfonamide

¹H-NMR (CDCl₃): δ 1.51 (t, 3H), 1.55 (s, 3H), 2.38-2.55 (br, 2H), 3.22-3.31 (br, 3H), 4.41-4.61 (br, 2H), 5.10-5.15 (br, 1H), 7.11-7.16 (m, 1H), 7.34-7.41 (m, 2H), 7.55-7.59 (m, 2H), 7.74-7.76 (m, 1H), 8.14-8.16 (m, 1H); MS: m/z 498.1 (MNa⁺).

Example 89

Compound 824 N-(3-Fluoropropyl)-N-(3-methyl-benzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

To a solution of compound 823 (100 mg, 0.237 mmol) in THF (9 mL), was added lithium hydroxide monohydrate (60 mg, 1.43 mmol) in water (3 mL), followed methanol (1 mL) at room temperature and the reaction mixture was stirred for 3 h. The reaction mixture was concentrated, triturated with 2N HCl, filtered, and the solids were washed three times with water, and the solid was dried under vacuum to afford 42 mg of compound 824. MS: m/z 408.0 (MH⁺).

Example 90

N-(4-Fluoro-3-trifluorobenzyl)-N-(3-chloro-benzo[b]thiophen-2-yl)-[N′-tert-butyloxycarbonyl]sulfonamide (309-A)

To a solution of compound 300-B (595 mg; 1.17 mmol) in DCE (6 mL), at ambient temperature, was added NCS (173 mg; 1.29 mmol), and the reaction mixture was allowed to stir at ambient temperature for 2 h. The reaction mixture was concentrated under reduced pressure and the crude residue purified by flash column chromatography (SiO₂) eluting with a heptane/EtOAc gradient to afford 528 mg of compound 309-A as a yellow solid. ¹H-NMR (DMSO-d₆): δ 1.51 (s, 9H), 5.07 (s, 2H), 7.42-7.47 (q, 1H), 7.51-7.55 (m, 2H), 7.64-7.68 (m, 1H), 7.75-7.79 (m, 2H), 8.01-8.03 (m, 1H), 11.83 (s, 1H).

N-(4-Fluoro-3-trifluorobenzyl)-N-(3-chloro-benzo[b]thiophen-2-yl)-N′-methyl-N-(tert-butyloxycarbonyl)-sulfonamide (309-B)

To a solution of compound 309-A (334 mg; 0.619 mmol) in DMF (3 mL), at ambient temperature, was added 60% NaH (31 mg; 0.805 mmol), and the suspension was allowed to stir at ambient temperature for 30 min. Methyl iodide (46 μL; 0.743 mmol) in DMF (0.1 mL), was added drop-wise, and the reaction was allowed to stir for 72 h at ambient temperature. The reaction mixture was diluted with EtOAc, washed with H₂O, brine, dried over Na₂SO₄, filtered, and the solvent evaporated under reduced pressure. The crude residue was purified by flash column chromatography (SiO₂) eluting with a heptane/EtOAc gradient to afford 303 mg of compound 309-B as a yellow oil. ¹H-NMR (DMSO-d₆): δ 1.54 (s, 9H), 3.02 (s, 3H), 5.10 (s, 2H), 7.44-7.49 (q, 1H), 7.52-7.55 (m, 2H), 7.65-7.69 (m, 1H), 7.76-7.79 (m, 2H), 8.02-8.04 (m, 1H); MS: m/z 453.0 ((M-Boc)+H⁺).

Compound 309 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-N′-methyl-sulfamide

To compound 309-B (303 mg, 0.548 mmol) was added solution of 1N HCl in dioxane (6 mL) and the reaction was stirred at ambient temperature for 18 h. The reaction mixture was evaporated under reduced pressure, the residue dried under vacuo, and purified by flash column chromatography (SiO₂) eluting with a heptane-EtOAc gradient to afford 211 mg of compound 309 as an oil ¹H-NMR (DMSO-d₆): δ 2.72 (s, 3H), 4.81 (s, 2H), 7.44-7.56 (m, 3H), 7.64-7.78 (m, 3H), 7.99-8.04 (m, 2H); MS: m/z 453.0 (MH⁺).

Following the procedure described above for Example 90 and substituting the appropriate reagents, starting materials and purification methods known to those skilled in the art, the following compounds of the present invention were prepared:

Compound 532 N-(Benzo[b]thiophen-2-yl)-N-(butyl)-N′-methyl-sulfamide

MS: m/z 299.1 (MH⁺).

Compound 533 N-(4-Fluoro-3-trifluoromethyl-benzyl)-N-(3-methylbenzo[b]thiophen-2-yl)-N′methyl-sulfamide

MS: m/z 433.0 (MH⁺).

Compound 553 N-(3-Chloro-benzo[b]thiophen-2-yl)-N-(butyl)-N′-methyl-sulfamide

MS: m/z 333.0 (MH⁺).

Compound 554 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(butyl)-N′-methyl-sulfamide

Compound 554 was synthesized from Example 90, step C, substituting NBS for NCS. MS: m/z 378.9 (MH⁺).

Compound 705 N-(3-Bromo-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-N′-methyl-sulfamide

Compound 705 was synthesized from Example 90, step C, substituting NBS for NCS. ¹H-NMR (CD₃OD): δ 2.83 (s, 3H), 7.16-7.20 (m, 1H), 7.41-7.79 (m, 6H); MS: m/z 499.0 (MH⁺).

Example 91

tert-Butyl-3-methylbenzo[b]thiophen-2-ylcarbamate (306-B)

A 5-L 4-neck flask equipped with an overhead mechanical stirrer, N₂ inlet/outlet adapter, reflux condenser, heating mantle and thermocouple was charged with t-butyl alcohol (2.11 L), compound 306-A (225.0 g, 1.17 mol), and diisopropylethylamine (225 mL, 1.29 mol). Diphenylphosphorylazide (304 mL, 1.4 mol) was premixed with toluene (300 mL) and then added drop-wise over 10 min. The reaction mixture was refluxed with stirring for 21 h, cooled to 22° C. and then evaporated in vacuo. The residue was dissolved in CH₂Cl₂ (1 L), washed with 1N NaOH (500 mL), brine (500 mL), the organic layer separated, dried over MgSO₄, filtered, and evaporated in vacuo to afford a dark orange oil (557 g). The crude residue was purified by the flash column chromatography (SiO₂) eluting with heptane-EtOAc to afford 265 g of compound 306-B as a pale yellow solid. ¹H-NMR (CDCl₃): δ 7.71 (d, 1H), 7.54 (d, 1H), 7.36-7.31 (m, 1H), 7.30-7.20 (m, 1H), 6.75 (br s, 1H), 2.23 (s, 3H), 1.55 (s, 9H).

3-Methylbenzo[b]thiophen-2-amine hydrochloride (757-A)

A 5-L 3-neck flask equipped with an overhead mechanical stirrer, N₂ inlet/outlet adapter, and thermocouple was charged with 4M HCl in dioxane (3.1 L), compound 306-B (265 g, 1.0 mol) and stirred for 18 h at 22° C. The white precipitate was collected by filtration, washed with diethyl ether (3×500 mL), and dried under house vacuum at 40° C. for 48 h to afford 174 g of compound 757-A as a white solid. ¹H-NMR (DMSO-d₆): δ 8.7 (br s, 3H), 7.71 (d, 1H), 7.44 (d, 1H), 7.29 (t, 1H), 7.14 (t, 1H), 2.184 (s, 3H).

N-(3-Methylbenzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide (306-C)

A 12-L 4-neck flask equipped with an overhead mechanical stirrer, N₂ inlet/outlet adapter, and thermocouple was charged with THF (3.26 L) and compound 757-A (326 g, 1.6 mol) followed by pyridine (265 mL, 3.3 mol). The reaction mixture was cooled to 5° C. using a ice bath, to which was added a solution of 4-(chlorosulfonyl)benzoic acid (396 g, 1.8 mol) dissolved in THF (2.44 L), drop-wise. The reaction was allowed to stir at ambient temperature for 72 h, diluted with EtOAc (4 L), washed with 1N HCl (1 L), brine (1 L), the organic layer dried over Na₂SO₄, filtered and evaporated under reduced pressure. The crude residue was purified by triturating with EtOAc/heptane (1:1/1 L). The slurry was filtered, washed with heptane (2×250 mL) and dried in a vacuum oven at 40° C. for 18 h to afford 470 g of compound 306-C as a white solid. ¹H-NMR (DMSO-d₆): δ 13.51 (br s, 1H), 10.65 (br s, 1H), 8.12 (d, 2H), 7.86 (d, 2H), 7.83-7.79 (m, 1H), 7.66-7.63 (m, 1H), 7.37-7.33 (m, 1H), 2.03 (s, 3H).

N-(3-Methylbenzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide (306-D)

A 12-L 4-neck flask equipped with an overhead mechanical stirrer, N₂ inlet/outlet adapter, and thermocouple was charged with MeOH (7.5 L) and compound 306-C (470 g, 1.35 mol). Sulfuric acid (24 mL, 0.45 mol) was added to the reaction mixture and the reaction was refluxed for 18 h. The reaction was cooled, diluted with EtOAc (4 L), washed with 1N NaOH (2 L), and H₂O (6 L). The aqueous layer with extracted with EtOAc (4×4 L), the combined organic extracts washed with brine (1 L), dried over Na₂SO₄, filtered and evaporated under reduced pressure to afford 306-D (crude material) as a red, thick oil. ¹H-NMR (DMSO-d₆): δ 7.89 (d, 2H), 7.81 (d, 2H), 7.41 (d, 1H), 7.16 (d, 1H), 7.09-7.04 (m, 1H), 6.91-6.85 (m, 1H), 3.82 (s, 3H), 1.99 (s, 3H).

A 5-L 3-neck flask equipped with an overhead mechanical stirrer, N₂ inlet/outlet adapter, and thermocouple was charged with the crude residue in H₂O (4 L). The solution was acidified with 1N HCl (200 mL) until the pH=1 and the reaction mixture allowed to stir for 30 min at ambient temperature. The solid was filtered, washed with H₂O (2×250 mL) and dried in a vacuum oven at 50° C. for 72 h to afford 302 g of compound 306-D as a white solid. ¹H-NMR (DMSO-d₆): δ 10.67 (br s, 1H), 8.13 (d, 2H), 8.00 (d, 2H), 7.90-7.77 (m, 1H), 7.64-7.61 (m, 1H), 7.36-7.32 (m, 2H), 3.89 (s, 3H), 2.02 (s, 3H).

Compound 141 N-[4-Fluoro-3-(trifluoromethyl)-benzyl]-N-(3-methylbenzo[b]thiophen-2-yl)-4-carbomethoxy-benzenesulfonamide

A 12-L 4-neck flask equipped with an overhead mechanical stirrer, N₂ inlet/outlet adapter, and thermocouple was charged with DMF (4.9 L), compound 306-D (245 g, 0.68 mol) and K₂CO₃ (112 g, 0.81 mol). 4-Fluoro-3-(trifluoromethyl)benzyl bromide (210 mL, 0.81 mol) was added drop-wise over 15 min and the reaction was stirred for 18 h at room temperature. The reaction mixture was poured into cold H₂O (10 L), stirred for 30 min, to which was added EtOAc (4 L). The layers were separated and the aqueous phase was extracted with EtOAc (2×1 L). The combined EtOAc layers were washed with brine (1 L), dried over Na₂SO₄, filtered and evaporated under reduced pressure. The crude product was purified using flash column chromatography (SiO₂) eluting with heptane-EtOAc to afford 269 g of compound 141 as a white solid. ¹H-NMR (DMSO-d₆) δ 8.21 (d, 2H), 8.03 (d, 2H), 7.86-7.83 (m, 1H), 7.71-7.63 (m, 3H), 7.45-7.37 (m, 3H), 4.89 (br s, 2H), 3.93 (s, 3H), 1.94 (s, 3H).

N-[4-Fluoro-3-(trifluoromethyl)-benzyl]-N-(3-methylbenzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide (not shown)

A 3-L 4-neck flask equipped with an overhead mechanical stirrer, N₂ inlet/outlet adapter, condenser and thermocouple was charged with MeOH (1.9 L) and compound 141 (190 g, 0.35 mol) followed by 3M NaOH (412 mL, 1.2 mol) and the reaction mixture was refluxed for 2 h. The reaction mixture was cooled to room temperature, diluted with EtOAc (2 L) and 1N HCl (2 L), the layers separated and the aqueous phase extracted with EtOAc (2 L). The organic extracts were combined, washed with brine (1.5 L), dried over Na₂SO₄, filtered and evaporated under reduced pressure. The yellow solid was placed in vacuum oven for 18 h at 50° C. to afford 158 g of the titled compound (not shown) as a yellow solid. ¹H-NMR (DMSO-d₆): δ 13.63 (s, 1H), 8.19 (d, 2H), 8.01 (d, 2H), 7.86-7.83 (m, 1H), 7.71-7.63 (m, 3H), 7.49-7.37 (M, 3H), 4.89 (br s, 1H), 1.95 (s, 3H).

Compound 306, Sodium Salt Sodium N-[4-Fluoro-3-(trifluoromethyl)-benzyl]-N-(3-methylbenzo[b]thiophen-2-yl)-4-carboxy-benzenesulfonamide

To a 5-L 4-neck flask equipped with an overhead mechanical stirrer, N₂ inlet/outlet adapter, and thermocouple, charged with MeOH (3.1 L) and the benzoic acid (310 g, 0.59 mol), was added 0.5M NaOMe in MeOH (1.25 L, 0.62 mol), the reaction was stirred for 1 h at ambient temperature and evaporated under reduced pressure to afford the crude sodium salt as a yellow solid. A 5-L 4-neck flask equipped with overhead mechanical stirrer, N₂ inlet/outlet adapter, condenser, and thermocouple, charged with crude sodium salt and IPA (3.3 L) was refluxed for 1 h and cooled to room temperature overnight. The resulting solid was filtered, washed with cold IPA (250 mL) and dried in a vacuum oven at 60° C. for 18 h, followed by 100° C. for 72 h to afford 250 g of compound 306 as a white solid. ¹H-NMR (DMSO-d₆): δ 8.04 (d, 2H), 7.85-7.82 (m, 1H), 7.76 (d, 2H), 7.69-7.63 (m, 3H), 7.48-7.41 (m, 1H), 7.40-7.35 (m, 2H), 4.83 (br s, 1H), 1.94 (s, 3H). Anal. Calcd for C₂₄H₁₆F₄NNaO₄S₂: C, 52.84; H, 2.96; N, 2.57; F, 13.93; S, 11.76; Na, 4.21. Found: C, 51.62; H, 2.70; N, 2.38; F, 13.73; S, 11.50; Na, 4.44; KF, 0.61.

Example 92

N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-carbomethoxy-benezenesulfonamide (496-A)

A 12-L 4-neck flask equipped with an overhead mechanical stirrer, N₂ inlet/outlet adapter, and thermocouple was charged with DMF (6.7 L), compound 306-D (334 g, 0.92 mol) and K₂CO₃ (153 g, 1.11 mol). 1-(Bromomethyl)-4-(trifluoromethoxy)benzene (178 mL, 1.11 mol) was added drop-wise over 15 min and the reaction mixture stirred for 5 h at room temperature. The reaction mixture was poured into cold H₂O (13 L) and stirred for 18 h. The resultant solid was filtered, washed with heptane (3×1 L), dried under vacuo for 18 h at 50° C., triturated with IPA (500 mL), filtered and dried under vacuo at 50° C. for 18 h to afford 318 g of compound 496-A as a white solid. ¹H-NMR (DMSO-d₆): δ 8.20 (d, 2H), 8.02 (d, 2H), 7.84-7.81 (m, 1H), 7.69-7.65 (m, 1H), 7.41-7.36 (m, 4H), 7.30 (d, 2H), 4.81 (br s, 2H), 3.93 (s, 3H), 1.90 (s, 3H). Anal. Calcd for C₂₅H₂₀F₃NO₅S₂: C, 56.07; H, 3.76; N, 2.62; F, 10.64; S, 11.97. Found: C, 55.85; H, 3.69; N, 2.72; F, 10.57; S, 11.65.

Compound 496, Sodium Salt Sodium N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-carboxy-benezenesulfonamide

To a 3-L 4-neck flask equipped with an overhead mechanical stirrer, N₂ inlet/outlet adapter, and thermocouple, charged with MeOH (1.0 L) and compound 496-A (100 g, 0.19 mol) was added 3M NaOH (68 mL, 0.21 mol) and the reaction was stirred for 1 h at 65° C. The reaction mixture was cooled and evaporated under reduced pressure to afford the sodium salt as a crude yellow solid. To the crude sodium salt was added IPA (250 mL) and the suspension heated (via a heat gun) until the mixture is homogeneous. The solution was allowed to cool slowly to ambient temperature, seeded with a previous batch of sodium compound 496, the resultant solid filtered, washed with cold IPA (150 mL) and dried in a vacuum oven at 60° C. for 18 h to afford 75 g of the sodium salt of compound 496 as a white solid. ¹H-NMR (DMSO-d₆): δ 8.03 (d, 2H), 7.84-7.81 (m, 1H), 7.74 (d, 2H), 7.67-7.64 (m, 1H), 7.40-7.33 (m, 4H), 7.30-7.27 (d, 2H), 4.76 (br s, 2H), 1.91 (s, 3H). Anal. Calcd for C₂₄H₁₉F₃NNaO₆S₂: C, 51.34; H, 3.41; N, 2.49; F, 10.15; S, 11.42; Na, 4.09; KF, 3.21. Found: C, 50.98; H, 3.10; N, 2.50; F, 9.25; S, 11.36; Na, 4.32; KF, 3.15.

Preparation of Intermediates Example 93 Preparation of Sulfonyl Chlorides Example 93A

3-Sulfo-benzoic acid methyl ester (Int-2)

To a suspension of compound Int-1 (5.09 g; 23.0 mmol) in DCM (50 mL), at ambient temperature, was added oxalyl chloride (2.41 mL; 27.6 mmol) in one-portion, followed by 1 drop of DMF and the reaction was stirred for 18 h at ambient temperature. MeOH was added to the reaction mixture and the reaction was allowed to stir for 72 h. The reaction solvent was evaporated under reduced pressure and the residue dried under vacuo to afford 4.97 grams of compound Int-2 as an oil.

3-Chlorosulfonyl-benzoic acid methyl ester (Int-3)

To compound Int-2 (4.97 g; 23.0 mmol) was added pyridine (20 mL) and the solution was stirred under N₂ for 60 min. Thionyl chloride (4.2 mL; 57.5 mmol) was added, drop-wise at ambient temperature, and the reaction was stirred at 55° C. for 2 h. The reaction was cooled, the solvent concentrated under reduced pressure and the liquid diluted with EtOAc. The organic phase was washed with 1 N HCl (3×), H₂O, brine, dried over Na₂SO₄, filtered and the solvent evaporated under reduced pressure to afford 4.89 g of compound Int-3 as a white solid. ¹H-NMR (DMSO-d₆): 3.87 (s, 3H), 7.44-7.58 (m, 1H), 7.81-7.98 (m, 2H), 8.17-8.27 (m, 1H), 14.50 (s, 1H).

Example 93B

1H-Benzimidazole-2-sulfonyl chloride (Int-5)

A suspension of 1H-benzimidazole-2-thiol, compound Int-4 (1.58 g; 10.5 mmol) in 20% v/v acetic acid water (30/90 mL) was cooled to 0° C. Chlorine gas was bubbled through the mixture until saturation, the reaction mixture was stirred for 1 h at 0° C., filtered, washed with ice-cold water and air dried to afford 2.2 g of compound Int-5 as an off-white solid.

Example 93C

5-Chloro-1-methyl-1H-benzimidazole-2-sulfonyl chloride (Int-7)

A suspension of 1-methyl-1H-benzimidazole-2-thiol, compound Int-6 (0.538 g; 3.27 mmol) in 20% v/v CCl₄/water (30/90 mL) was cooled to 0° C. Chlorine gas was bubbled through the mixture until saturation, the reaction mixture was stirred for 1 h at 0° C., filtered, washed with ice-cold water and air dried to afford 0.5 g of compound Int-7 as a white solid.

Example 94 General 4-cyanopyridyl Intermediates

Compound Int-8, was prepared by the method used to synthesize Cpd 757 in Example 30, step A, and Example 3, step A.

N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(5,5,5-trifluoro-pentyl)-4-cyano-pyridin-3-ylsulfonamide (Int-9)

A solution of compound Int-8 (0.250 g, 0.54 mmol), dimethylformamide (2 mL), potassium cyanide (0.07 g, 1.08 mmol), and 18-crown-6 ether (0.006 g, 0.022 mmol) was refluxed for 4 h. The reaction mixture was cooled, poured over ice-water and extracted with EtOAc. The solvent was evaporated in vacuo, and the crude residue concentrated to afford 0.25 g of compound Int-9 as a dark gum. MS: m/z 454.0 (MH⁺).

Example 95 General Synthesis of Benzyl Bromide Intermediates Example 95A

4-Bromomethyl-1,2-dimethoxy-benzene (Int-11)

To a stirred solution of Int-10 (1.0 g, 5.95 mmol) in dichloromethane (10 mL), cooled to 0° C., was added phosphorous tribromide (1.93 g, 7.13 mmol), drop-wise, and the reaction was stirred for 2 h. The reaction was quenched with aqueous NH₄Cl, the organic phase separated, dried over Na₂SO₄, filtered, and the solvent evaporated in vacuo to afford 1.0 g of compound Int-11. ¹H-NMR (DMSO-d₆) δ 3.74 (s, 3H), 3.72 (s, 3H), 4.41 (d, 2H), 6.83 (d, 1H), 6.85-6.94 (m, 2H).

Example 95B

(4-Trifluoromethanesulfonyl-phenyl)-methanol (Int-13)

To a solution of compound Int-12 (2.08 g, 10.0 mmol) in trifluoroacetic acid (25 mL) was added a 30% H₂O₂ (5 mL) solution. After stirring at ambient temperature for 5 days, the reaction mixture was diluted with ice-water (125 mL). A scoop of 10% Pd/C was added to consume the excess H₂O₂ present and allowed to stir overnight. The mixture was extracted with diethyl ether (3×50 mL), the combined organics washed times with saturated NaHCO₃ solution (4×50 mL) then treated with solid NaHCO₃ until neutralized. The layers were separated and the organic phase was washed with a 10% Na₂SO₃ solution (50 mL), brine (50 mL), dried with Na₂SO₄, filtered, and evaporated in vacuo to afford 2.19 g of compound Int-13 as a white solid. ¹H-NMR (DMSO-d₆) δ 4.70 (s, 2H), 5.62 (br s, 1H), 7.80 (d, 2H), 8.10 (d, 2H).

1-Bromomethyl-4-trifluoromethanesulfonyl-benzene (Int-14)

To a solution of compound Int-13 (2.18 g, 9.05 mmol) in diethyl ether (25 mL) was added PBr₃ (1.3 mL, 13.7 mmol). The reaction was stirred under a nitrogen atmosphere for 3 days, diluted with diethyl ether (100 mL) and washed with H₂O (2×50 mL), saturated NaHCO₃ solution (50 mL), brine (50 mL), dried over Na₂SO₄, filtered and evaporated in vacuo to afford 2.65 g of compound Int-14 as an off-white solid. ¹H-NMR (CDCl₃): δ 4.53 (s, 2H), 7.69 (d, 2H), 8.03 (d, 2H).

Example 96 Preparation of 1-(1H-imidazol-2-yl)-N,N-dimethylmethanamine Intermediate

1-(1H-imidazol-2-yl)-N,N-dimethylmethanamine (Int-16)

A solution of compound Int-15 (5.0 g, 52.03 mmole), MeOH (10 mL), H₂O (15 mL), and dimethylamine (25 mL, 50 mmole) was stirred at 22° C. for 2 h. The reaction mixture was cooled to 0° C., stirred for 20 min, to which was added NaBH₄ (5.0 g, 139.9 mmole) in one-portion and the reaction was heated at 56° C. for 3 h. The reaction mixture was cooled, quenched with brine (100 mL), extracted with CH₂Cl₂ (100 mL), dried over MgSO₄, filtered, and the solvent evaporated in vacuo to afford 4.0 g of compound Int-16 as a yellow waxy solid. ¹H-NMR (CDCl₃): δ 2.20 (s, 6H), 3.50 (s, 2H), 6.90 (s, 2H), 10.10 (br s, 1H); MS: m/z 125.2 (MH⁺).

Example 97 General Sodium Salt Preparation

Compound 784, Sodium Salt Sodium, N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl-4-(5-oxo-4,5-dihydro-[1,2,4]thiadiazol-3-yl)-benzenesulfonamide

To a solution of compound 784 (335.7 mg; 0.579 mmol) suspended in MeOH (10 mL) was added a solution of 0.117 M NaOMe (5.2 mL) and the solution was stirred for 30 min. The solvent was evaporated under reduced pressure and dried under vacuo at 50° C. to afford 353.8 mg of the sodium salt of compound 784 as a white solid. ¹H-NMR (DMSO-d₆): δ 3.34 (s, 3H), 4.88 (br s, 2H), 7.35-7.43 (m, 2H), 7.45-7.47 (t, 1H), 7.54-7.68 (m, 4H), 7.83-7.85 (m, 3H), 8.20-8.22 (d, 2H); MS: m/z 580.0 (MH⁺).

Using the methods described in the schemes and specific examples, and adaptations thereof, compounds of Formula (I) shown in Table 1 were prepared.

TABLE 1 Cpd No. G Y R¹ R² R³ R⁴ R⁵ R⁶ A B 1 S H phenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 2 S methyl 1-methyl-1H- 3,4- H H H H CR⁵ CR⁶ imidazol-4-yl difluorophenylmethyl 3 S H phenyl 3-fluorophenylmethyl H H H H CR⁵ CR⁶ 4 S Cl phenyl 4-fluorophenylmethyl H H H H CR⁵ CR⁶ 5 S Cl phenyl quinolin-8-ylmethyl H H H H CR⁵ CR⁶ 6 S Cl phenyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 7 S Cl phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 8 S Cl phenyl 4-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 9 S H pyridin-2-yl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 10 S methyl 1-methyl-1H- quinolin-8-ylmethyl H H H H CR⁵ CR⁶ imidazol-4-yl 11 S methyl 1-methyl-1H- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ imidazol-4-yl 12 S methyl pyridin-3-yl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 13 S methyl pyridin-3-yl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 14 S methyl pyridin-3-yl quinolin-8-ylmethyl H H H H CR⁵ CR⁶ 15 S methyl thien-3-yl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 16 S methyl thien-3-yl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 17 S methyl thien-3-yl quinolin-8-ylmethyl H H H H CR⁵ CR⁶ 18 S methyl benzo[b]thiophen- 3,4- H H H H CR⁵ CR⁶ 2-yl difluorophenylmethyl 19 S methyl benzo[b]thiophen- quinolin-8-ylmethyl H H H H CR⁵ CR⁶ 2-yl 20 S methyl quinolin-8-yl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 21 S methyl quinolin-8-yl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 22 S methyl quinolin-8-yl quinolin-8-ylmethyl H H H H CR⁵ CR⁶ 23 S Cl phenyl 3-fluorophenylmethyl H H H H CR⁵ CR⁶ 24 S Cl phenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 25 S methyl 3- 3,4- H H H H CR⁵ CR⁶ methoxyphenyl difluorophenylmethyl 26 S methyl 4- 3,4- H H H H CR⁵ CR⁶ methoxyphenyl difluorophenylmethyl 27 S methyl isoquinolin-5-yl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 28 S methyl isoquinolin-5-yl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 29 S methyl isoquinolin-5-yl quinolin-8-ylmethyl H H H H CR⁵ CR⁶ 30 S methyl quinolin-6-yl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 31 S methyl quinolin-6-yl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 32 S methyl quinolin-6-yl quinolin-8-ylmethyl H H H H CR⁵ CR⁶ 33 S H pyridin-3-yl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 34 S H methyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 35 S H ethyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 36 S H n-propyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 37 S H n-butyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 38 S methyl thien-2-yl 4-trifluoromethyl- H H H H CR⁵ CR⁶ 3-fluorophenylmethyl 39 S methyl pyridin-3-yl 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 40 S methyl ethyl 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 41 S methyl ethyl 3,4-difluorophenylmethyl H H H H CR⁵ CR⁶ 42 S methyl ethyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 43 S H ethyl 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 44 S methyl dimethylamino 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 45 S H methyl 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 46 S H phenyl 4-chlorophenylmethyl H H H H CR⁵ CR⁶ 47 S H phenyl 2-methoxyphenylmethyl H H H H CR⁵ CR⁶ 48 S H phenyl 3-methoxyphenylmethyl H H H H CR⁵ CR⁶ 49 S H phenyl 4-methoxyphenylmethyl H H H H CR⁵ CR⁶ 50 S H phenyl 2-fluorophenylmethyl H H H H CR⁵ CR⁶ 51 S H phenyl 3-nitrophenylmethyl H H H H CR⁵ CR⁶ 52 S H phenyl pyridin-2-ylmethyl H H H H CR⁵ CR⁶ 53 S H phenyl pyridin-3-ylmethyl H H H H CR⁵ CR⁶ 54 S H phenyl pyridin-4-ylmethyl H H H H CR⁵ CR⁶ 55 S H phenyl 2-nitrophenylmethyl H H H H CR⁵ CR⁶ 56 S H phenyl 2-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 57 S H phenyl 3-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 58 S H phenyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 59 S H phenyl phenylmethyl H H H H CR⁵ CR⁶ 60 S H phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ methoxyphenylmethyl 61 S H phenyl 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 62 S H phenyl 2-methylphenylmethyl H H H H CR⁵ CR⁶ 63 S H phenyl 3-methylphenylmethyl H H H H CR⁵ CR⁶ 64 S methyl 4-methoxy-3- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ fluorophenyl 65 S methyl benzothiazol-6- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ yl 66 S methyl 2-oxo-2,3- 4-fluoro-3- H H H H CR⁵ CR⁶ dihydro-benzooxazol- trifluoromethylphenylmethyl 6-yl 67 S methyl 3-oxo-3,4- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ dihydro-2H- benzo[1,4]oxazin- 6-yl 68 S methyl 4-methyl-3,4- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ dihydro-2H- benzo[1,4]oxazin- 7-yl 69 S methyl 4-[1,2,3]thiadiazol- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 4-yl- phenyl 70 S methyl 3- 4-fluoro-3- H H H H CR⁵ CR⁶ phenoxyphenyl trifluoromethylphenylmethyl 71 S methyl 2-(methoxycarbonyl)ethyl 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 72 S methyl 2,4-dihydroxy- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 6-methyl- pyrimidin-5-yl 73 S methyl 2-(2,2,2- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ trifluoro-acetyl)- 1,2,3,4- tetrahydro- isoquinolin-8-yl 74 S methyl 1,3,5-trimethyl- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 1H-pyrazol-4-yl 75 S methyl 2,4-dimethyl- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ thiazol-5-yl 76 S methyl 2-chloropyridin- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 5-yl 77 S methyl 2-chloropyridin- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 3-yl 78 S H thien-3-yl 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ 79 S methyl 1,2,3,4- 4-fluoro-3-trifluoromethylphenylmethyl H H H H CR⁵ CR⁶ tetrahydro- isoquinolin-8-yl 80 S Cl phenyl cyclohexylmethyl H H H H CR⁵ CR⁶ 81 S Cl phenyl 2-(tert-butoxy)ethyl H H H H CR⁵ CR⁶ 82 S Cl phenyl 2-(2-oxo- H H H H CR⁵ CR⁶ pyrrolidin-1-yl)ethyl 83 S Cl phenyl n-butyl H H H H CR⁵ CR⁶ 84 S Cl phenyl allyl H H H H CR⁵ CR⁶ 85 S Cl phenyl 2-(phenyl)ethyl H H H H CR⁵ CR⁶ 86 S Cl phenyl 2-(tert- H H H H CR⁵ CR⁶ butoxycarbonylamino)ethyl 87 S Cl phenyl 2- H H H H CR⁵ CR⁶ (dimethylamino)ethyl 88 S Cl phenyl 2- H H H H CR⁵ CR⁶ (methanesulfonyl)ethyl 89 S Cl phenyl (N-tert- H H H H CR⁵ CR⁶ butoxycarbonylpyrrolidin- 2-yl)methyl 90 S Cl phenyl (N-tert- H H H H CR⁵ CR⁶ butoxycarbonylpiperidin- 4-yl)methyl 91 S Cl phenyl 2-(2-oxo- H H H H CR⁵ CR⁶ imidazolidin-1-yl)ethyl 92 S Cl phenyl 2- H H H H CR⁵ CR⁶ (morpholin-4-yl)ethyl 93 S methyl phenyl 2-(methoxycarbonyl)- H H H H CR⁵ CR⁶ 2(R)-methylethyl 94 S methyl phenyl 2-(methoxycarbonyl)- H H H H CR⁵ CR⁶ 2(S)-methylethyl 95 S methyl phenyl 2-(morpholin-4- H H H H CR⁵ CR⁶ yl)ethyl 96 S methyl phenyl 2-(piperidin-1-yl)ethyl H H H H CR⁵ CR⁶ 97 S methyl phenyl cyclopropylmethyl H H H H CR⁵ CR⁶ 98 S methyl phenyl 2- H H H H CR⁵ CR⁶ (methylsulfanyl)ethyl 99 S methyl phenyl 2-methoxyethyl H H H H CR⁵ CR⁶ 100 S methyl phenyl 2-(tert-butoxy)ethyl H H H H CR⁵ CR⁶ 101 S methyl phenyl methoxycarbonylmethyl H H H H CR⁵ CR⁶ 102 S methyl phenyl 2,2-difluoroethyl H H H H CR⁵ CR⁶ 103 S methyl phenyl (N-tert- H H H H CR⁵ CR⁶ butoxycarbonylpyrrolidin- 2-yl)methyl 104 S methyl phenyl 2-phenylethyl H H H H CR⁵ CR⁶ 105 S methyl ethyl 2-methoxyethyl H H H H CR⁵ CR⁶ 106 S methyl ethyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 107 S methyl ethyl pent-3-ynyl H H H H CR⁵ CR⁶ 108 S methyl ethyl 2- H H H H CR⁵ CR⁶ (methylsulfanyl)ethyl 109 S methyl ethyl 2-oxo-pyrrolidin- H H H H CR⁵ CR⁶ 5(S)-ylmethyl 110 S methyl ethyl 2-(tert-butoxy)ethyl H H H H CR⁵ CR⁶ 111 S methyl ethyl 2,2-difluoroethyl H H H H CR⁵ CR⁶ 112 S methyl ethyl cyclopropylmethyl H H H H CR⁵ CR⁶ 113 S methyl ethyl 2-(morpholin-4-yl)ethyl H H H H CR⁵ CR⁶ 114 S methyl ethyl (N-tert- H H H H CR⁵ CR⁶ butoxycarbonylpyrrolidin- 2-yl)methyl 115 S H phenyl 2-phenylethyl H H H H CR⁵ CR⁶ 116 S H phenyl allyl H H H H CR⁵ CR⁶ 117 S H phenyl n-butyl H H H H CR⁵ CR⁶ 118 S H phenyl cyclohexylmethyl H H H H CR⁵ CR⁶ 119 S H phenyl cyclohexyl H H H H CR⁵ CR⁶ 120 S H phenyl 2- H H H H CR⁵ CR⁶ (methylsulfanyl)ethyl 121 S acetyl ethyl n-butyl H H H H CR⁵ CR⁶ 122 S acetyl ethyl cyclopropylmethyl H H H H CR⁵ CR⁶ 123 S acetyl ethyl 2-(tert-butoxy)ethyl H H H H CR⁵ CR⁶ 124 S acetyl ethyl 2-(morpholin-4-yl)ethyl H H H H CR⁵ CR⁶ 125 S methyl phenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 126 S methyl phenylmethyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 127 S methyl 3-fluorophenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 128 S methyl 2-fluorophenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 129 S methyl thien-2-yl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 130 S H 1-methyl-1H- 3,4- H H H H CR⁵ CR⁶ imidazol-4-yl difluorophenylmethyl 131 S H 3-fluorophenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 132 S H 4- 3,4- H H H H CR⁵ CR⁶ trifluoromethylphenyl difluorophenylmethyl 133 S H methanesulfonylmethyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 134 S H 4- 4-fluoro-3- H H H H CR⁵ CR⁶ methoxyphenyl trifluoromethylphenylmethyl 135 S H 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 136 S H 3-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 137 S methyl 3-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 138 S methyl 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 139 S H 2-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 140 S Br phenyl 4-fluorophenylmethyl H H H H CR⁵ CR⁶ 141 S Br pyridin-3-yl 3,4- H OCH₃ H H CR⁵ CR⁶ difluorophenylmethyl 142 S H phenyl 3,4- H H H OCH₃ CR⁵ CR⁶ difluorophenylmethyl 143 S Cl phenyl 3,4- H H H OCH₃ CR⁵ CR⁶ difluorophenylmethyl 144 S Cl phenyl 3,4- H Cl H OCH₃ CR⁵ CR⁶ difluorophenylmethyl 145a S Br phenyl 3,4- H H NA H N CR⁶ difluorophenylmethyl 145b S Cl phenyl 3,4- H H NA H N CR⁶ difluorophenylmethyl 146 S H phenyl 4-fluoro-3- H H NA H N CR⁶ trifluoromethylphenylmethyl 147 S H phenyl 3,4- H H H NA CR⁵ N difluorophenylmethyl 148 S Br phenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 149 S Br pyridin-3-yl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 150 S Br 1-methyl-1H- 3,4- H H H H CR⁵ CR⁶ imidazol-4-yl difluorophenylmethyl 151 S Br methyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 152 S Br ethyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 153 S Br n-propyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 154 S Br n-butyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 155 S Br 3-fluorophenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 156 S Br 4- 3,4- H H H H CR⁵ CR⁶ trifluoromethylphenyl difluorophenylmethyl 157 S Br methyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 158 S Cl phenyl 4- H H H H CR⁵ CR⁶ chlorophenylmethyl 159 S Br phenyl 4- H H H H CR⁵ CR⁶ chlorophenylmethyl 160 S Br phenyl 2- H H H H CR⁵ CR⁶ methoxyphenylmethyl 161 S Br phenyl 5-bromo-2- H H H H CR⁵ CR⁶ methoxyphenylmethyl 162 S Br phenyl 3-methoxyphenylmethyl H H H H CR⁵ CR⁶ 163 S Br phenyl 2-bromo-5- H H H H CR⁵ CR⁶ methoxyphenylmethyl 164 S Br phenyl 4-methoxyphenylmethyl H H H H CR⁵ CR⁶ 165 S Br phenyl 4-methoxy-3- H H H H CR⁵ CR⁶ bromophenylmethyl 166 S Br phenyl 2-fluorophenylmethyl H H H H CR⁵ CR⁶ 167 S Br phenyl 3-nitrophenylmethyl H H H H CR⁵ CR⁶ 168 S Br phenyl pyridin-2-ylmethyl H H H H CR⁵ CR⁶ 169 S Br phenyl pyridin-3-ylmethyl H H H H CR⁵ CR⁶ 170 S Br phenyl pyridin-4-ylmethyl H H H H CR⁵ CR⁶ 171 S Br phenyl 2-nitrophenylmethyl H H H H CR⁵ CR⁶ 172 S Br phenyl 2-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 173 S Br phenyl 3-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 174 S Br phenyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 175 S Br phenyl phenylmethyl H H H H CR⁵ CR⁶ 176 S Br phenyl 4-fluoro-3-methoxyphenylmethyl H H H H CR⁵ CR⁶ 177 S Br phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 178 S Br phenyl 2- H H H H CR⁵ CR⁶ methylphenylmethyl 179 S Br phenyl 3- H H H H CR⁵ CR⁶ methylphenylmethyl 180 S Cl 3- 4-fluoro-3- H H H H CR⁵ CR⁶ methoxyphenyl trifluoromethylphenylmethyl 181 S Cl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ methoxyphenyl trifluoromethylphenylmethyl 182 S Br 4- 4-fluoro-3- H H H H CR⁵ CR⁶ methoxyphenyl trifluoromethylphenylmethyl 183 S Br ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 184 S Br thien-2-yl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 185 S Br 3- 4-fluoro-3- H H H H CR⁵ CR⁶ methoxyphenyl trifluoromethylphenylmethyl 186 S Br thien-3-yl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 187 S Cl thien-3-yl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 188 S Br pyridin-3-yl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 189 S Cl pyridin-3-yl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 190 S Cl ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 191 S Cl thien-2-yl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 192 S Br 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 193 S Br 3-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 194 S Cl 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 195 S Cl 3-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 196 S Cl 2-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 197 S Br 2-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 198 S cyano ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 199 S pyrimidin- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ 5-yl trifluoromethylphenylmethyl 200 S 2-fluorophenyl ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 201 S 4-fluorophenyl ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 202 S thien-3- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ yl trifluoromethylphenylmethyl 203 S acetyl ethyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 204 S acetyl phenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 205 S acetyl ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 206 S formyl phenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 207 S formyl phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 208 S formyl methyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 209 S formyl methyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 210 S formyl ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 211 S formyl 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 212 S formyl ethyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 213 S hydroxymethyl phenyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 214 S hydroxymethyl phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 215 S hydroxymethyl methyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 216 S hydroxymethyl methyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 217 S hydroxymethyl ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 218 S hydroxymethyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 219 S hydroxymethyl ethyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 220 S 1- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxyethyl trifluoromethylphenylmethyl 221 S 1- ethyl 3,4- H H H H CR⁵ CR⁶ hydroxyethyl difluorophenylmethyl 222 S 1- phenyl 3,4- H H H H CR⁵ CR⁶ hydroxyethyl difluorophenylmethyl 223 S 1- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxyethyl trifluoromethylphenylmethyl 224 S 1- methyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- trifluoromethylphenylmethyl ethyl 225 S 1- methyl 3,4- H H H H CR⁵ CR⁶ hydroxy- difluorophenylmethyl ethyl 226 S 1- ethyl 3,4- H H H H CR⁵ CR⁶ hydroxy- difluorophenylmethyl 1- methyl- ethyl 227 S 1- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- trifluoromethylphenylmethyl 1- methyl- ethyl 228 S acetyl methyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 229 S acetyl methyl 3,4- H H H H CR⁵ CR⁶ difluorophenylmethyl 230 S Br phenyl 5-(ethoxycarbonyl)pentyl H H H H CR⁵ CR⁶ 231 S Br phenyl n-butyl H H H H CR⁵ CR⁶ 232 S Br phenyl cyclohexylmethyl H H H H CR⁵ CR⁶ 233 S Br phenyl 2-phenylethyl H H H H CR⁵ CR⁶ 234 S Br phenyl 2-(tert-butoxy)ethyl H H H H CR⁵ CR⁶ 235 S Br phenyl 2(R)-3-dihydroxy- H H H H CR⁵ CR⁶ propyl 236 S Br phenyl 2-(2-oxo- H H H H CR⁵ CR⁶ pyrrolidin-1-yl)ethyl 237 S Br phenyl 2- H H H H CR⁵ CR⁶ (morpholin-4-yl)ethyl 238 S Br phenyl 2- H H H H CR⁵ CR⁶ (dimethylamino)ethyl 239 S Br phenyl 2-(methanesulfonyl)ethyl H H H H CR⁵ CR⁶ 240 S Br phenyl 2-(2-oxo- H H H H CR⁵ CR⁶ imidazolidin-1-yl)- ethyl 241 S Br phenyl N-methylpyrrolidin- H H H H CR⁵ CR⁶ 2(S)-ylmethyl 242 S Br phenyl 2,2-difluoroethyl H H H H CR⁵ CR⁶ 243 S Br phenyl methoxycarbonylmethyl H H H H CR⁵ CR⁶ 244 S Br phenyl 2(S)- H H H H CR⁵ CR⁶ methoxycarbonyl-2- methylethyl 245 S Br phenyl 2(R)- H H H H CR⁵ CR⁶ methoxycarbonyl-2- methylethyl 246 S Br phenyl 3-phenylpropyl H H H H CR⁵ CR⁶ 247 S Br phenyl ethyl H H H H CR⁵ CR⁶ 248 S Br phenyl n-hexyl H H H H CR⁵ CR⁶ 249 S Br phenyl adamant-1-ylmethyl H H H H CR⁵ CR⁶ 250 S Br phenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 251 S Br phenyl pent-3-ynyl H H H H CR⁵ CR⁶ 252 S Br phenyl 2-methoxyethyl H H H H CR⁵ CR⁶ 253 S Br phenyl 3-(methylcarbonyl)propyl H H H H CR⁵ CR⁶ 254 S Br phenyl 2-(dimethylphospho)ethyl H H H H CR⁵ CR⁶ 255 S Br phenyl cyclopropylmethyl H H H H CR⁵ CR⁶ 256 S Br phenyl 2- H H H H CR⁵ CR⁶ (piperidin-1-yl)ethyl 257 S Br phenyl 2-(2,5-dioxo- H H H H CR⁵ CR⁶ pyrrolidin-1-yl)ethyl 258 S Br phenyl 2-oxo-pyrrolidin- H H H H CR⁵ CR⁶ 5(R)-ylmethyl 259 S Br phenyl 2-oxo-pyrrolidin- H H H H CR⁵ CR⁶ 5(S)-ylmethyl 260 S Br phenyl 2- H H H H CR⁵ CR⁶ (methylsulfanyl)ethyl 261 S Br ethyl n-butyl H H H H CR⁵ CR⁶ 262 S Br ethyl cyclopropylmethyl H H H H CR⁵ CR⁶ 263 S Br ethyl 2,2-difluoroethyl H H H H CR⁵ CR⁶ 264 S Br ethyl 2-(tert-butoxy)ethyl H H H H CR⁵ CR⁶ 265 S Br dimethylamino n-butyl H H H H CR⁵ CR⁶ 266 S Br dimethylamino cyclopropylmethyl H H H H CR⁵ CR⁶ 267 S Br dimethylamino 2-(tert-butoxy)ethyl H H H H CR⁵ CR⁶ 268 S Br dimethylamino 2,2-difluoroethyl H H H H CR⁵ CR⁶ 269 S Br dimethylamino 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 270 S Cl phenyl 2-aminoethyl H H H H CR⁵ CR⁶ 271 S Br 4- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ carboxyphenyl 272 S Br 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 273 S Br 4- cyclopropylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 274 S Br 4- 2-methoxyethyl H H H H CR⁵ CR⁶ carboxyphenyl 275 S Br 4- 2-(tert-butoxy)ethyl H H H H CR⁵ CR⁶ carboxyphenyl 276 S Br 4- 2,2-difluoroethyl H H H H CR⁵ CR⁶ carboxyphenyl 277 S Br 4- 2- H H H H CR⁵ CR⁶ carboxyphenyl (morpholin-4-yl)ethyl 278 S Br 4- adamant-1-ylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 279 S Br 4- cyclohexylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 280 S 1- ethyl n-butyl H H H H CR⁵ CR⁶ hydroxyethyl 281 S 1- ethyl cyclopropylmethyl H H H H CR⁵ CR⁶ hydroxyethyl 282 S 1- ethyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ hydroxyethyl 283 S 1- ethyl 2-(tert-butoxy)ethyl H H H H CR⁵ CR⁶ hydroxyethyl 284 S 1- ethyl 2- H H H H CR⁵ CR⁶ hydroxyethyl (morpholin-4-yl)ethyl 285 S methyl 4- 3,4- H H H H CR⁵ CR⁶ hydroxyphenyl difluorophenylmethyl 286 S methyl 3- 3,4- H H H H CR⁵ CR⁶ hydroxyphenyl difluorophenylmethyl 287 S H phenyl 3- H H H H CR⁵ CR⁶ hydroxyphenylmethyl 288 S Cl 3- 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxyphenyl trifluoromethylphenylmethyl 289 S Cl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxyphenyl trifluoromethylphenylmethyl 290 S Br 4- 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxyphenyl trifluoromethylphenylmethyl 291 S Br 3- 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxyphenyl trifluoromethylphenylmethyl 292 S Br 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 293 S Br 3- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 294 S Cl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 295 S H 3- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 296 S H 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 297 S Cl 2- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 298 S Br 2- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 299 S formyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 300 S H amino 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 301 S Br amino 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 302 S Cl amino 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 303 S bromo amino cyclopropylmethyl H H H H CR⁵ CR⁶ 304 S bromo amino 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 305 S methyl 3- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 306 S methyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 307 S chloro 3- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 308 S H 4- 4-fluoro-3- H H H H CR⁵ CR⁶ methylcarbonylphenyl trifluoromethylphenylmethyl 309 S chloro methylamino 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 310 S H 2-chloropyridin- 4-fluoro-3- H H H H CR⁵ CR⁶ 3-yl trifluoromethylphenylmethyl 311 S H 6-chloro- 4-fluoro-3- H H H H CR⁵ CR⁶ pyridin-3-yl trifluoromethylphenylmethyl 312 S bromo 4- 4-fluoro-3- H H H H CR⁵ CR⁶ methylcarbonylphenyl trifluoromethylphenylmethyl 313 S methylcarbonyl 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 314 S methylcarbonyl phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 315 S H dimethylamino 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 316 S 1- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- trifluoromethylphenylmethyl 1- methyl- ethyl 317 S bromo dimethylamino 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 318 S methylcarbonyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 319 S bromo 2-chloropyridin- 4-fluoro-3- H H H H CR⁵ CR⁶ 3-yl trifluoromethylphenylmethyl 320 S bromo 6-chloro- 4-fluoro-3- H H H H CR⁵ CR⁶ pyridin-3-yl trifluoromethylphenylmethyl 321 S chloro 2-chloropyridin- 4-fluoro-3- H H H H CR⁵ CR⁶ 3-yl trifluoromethylphenylmethyl 322 S bromo pyridin-3-yl 3-fluoro-4- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 323 S bromo pyridin-3-yl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 324 S bromo pyridin-3-yl 3-chloro-6- H H H H CR⁵ CR⁶ fluorophenylmethyl 325 S trifluoromethyl phenyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 326 S methyl 5-(2-methyl-5- 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethyl- trifluoromethylphenylmethyl 2H-pyrazol-3- yl)-thien-2-yl 327 S methyl 5-methoxycarbonyl- 4-fluoro-3- H H H H CR⁵ CR⁶ furan-2-yl trifluoromethylphenylmethyl 328 S methyl 1-methyl-3- 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethyl- trifluoromethylphenylmethyl 1H-pyrazol-4-yl 329 S methyl 5-(5- 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethyl- trifluoromethylphenylmethyl isoxazol-3-yl)- thien-2-yl 330 S methyl 5-bromo-6- 4-fluoro-3- H H H H CR⁵ CR⁶ chloro- trifluoromethylphenylmethyl pyridin-3-yl 331 S methyl 5,6-dichloro- 4-fluoro-3- H H H H CR⁵ CR⁶ pyridin-3-yl trifluoromethylphenylmethyl 332 S methyl 4-(pyrazol-1- 4-fluoro-3- H H H H CR⁵ CR⁶ yl)phenyl trifluoromethylphenylmethyl 333 S methyl 3-(5-methyl- 4-fluoro-3- H H H H CR⁵ CR⁶ [1,3,4]oxadiazol- trifluoromethylphenylmethyl 2-yl)phenyl 334 S methyl 4-(oxazol-5-yl)phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 335 S 1- 4- 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- carboxyphenyl trifluoromethylphenylmethyl ethyl 336 S methyl 3-chloro-4- 4-fluoro-3- H H H H CR⁵ CR⁶ methylcarbonylamino- trifluoromethylphenylmethyl phenyl 337 S methyl 6-chloro- 4-fluoro-3- H H H H CR⁵ CR⁶ imidazo[2,1-b]thiazol- trifluoromethylphenylmethyl 5-yl 338 S chloro 6-chloro- 4-fluoro-3- H H H H CR⁵ CR⁶ pyridin-3-yl trifluoromethylphenylmethyl 339 S methylcarbonyl 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ 340 S H pyridin-3-yl n-butyl H H H H CR⁵ CR⁶ 341 S 1- 4-(1-hydroxy-1- n-butyl H H H H CR⁵ CR⁶ hydroxy- methyl-ethyl)phenyl 1- methyl- ethyl 342 S methylcarbonyl 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 343 S 1- 4- n-butyl H H H H CR⁵ CR⁶ hydroxy- carboxyphenyl 1- methyl- ethyl 344 S 1- 4- n-butyl H H H H CR⁵ CR⁶ hydroxy- methylcarbonylphenyl 1- methyl- ethyl 345 S bromo pyridin-3-yl n-butyl H H H H CR⁵ CR⁶ 346 S dimethylamino- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ methyl trifluoromethylphenylmethyl 347 S methylamino- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ methyl trifluoromethylphenylmethyl 348 S n-propylamino- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ methyl trifluoromethylphenylmethyl 349 S pyrrolidin- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ 1-ylmethyl trifluoromethylphenylmethyl 350 S bromo methanesulfonyl- 4-fluoro-3- H H H H CR⁵ CR⁶ methyl trifluoromethylphenylmethyl 351 S methyl 4- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ methylcarbonylphenyl 352 S methyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ methylcarbonylphenyl trifluoromethylphenylmethyl 353 S methyl 3-(2-methyl- 4-fluoro-3- H H H H CR⁵ CR⁶ pyrimidin-4-yl)phenyl trifluoromethylphenylmethyl 354 S methyl 3-(2-methyl- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ pyrimidin-4-yl)phenyl 355 S methyl 8-methoxy- 4-fluoro-3- H H H H CR⁵ CR⁶ quinolin-5-yl trifluoromethylphenylmethyl 356 S methyl 8-methoxy- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ quinolin-5-yl 357 S methyl 2-methoxypyridin- 4-fluoro-3- H H H H CR⁵ CR⁶ 3-yl trifluoromethylphenylmethyl 358 S methyl 2- 4-fluoro-3- H H H H CR⁵ CR⁶ dimethylaminopyridin- trifluoromethylphenylmethyl 3-yl 359 S methyl 6-methoxypyridin- 4-fluoro-3- H H H H CR⁵ CR⁶ 3-yl trifluoromethylphenylmethyl 360 S methyl 6- 4-fluoro-3- H H H H CR⁵ CR⁶ dimethylamino- trifluoromethylphenylmethyl pyridin-3-yl 361 S 1- 4- 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- carboxyphenyl trifluoromethylphenylmethyl 1- methyl- ethyl 362 S H methanesulfonyl- 4-fluoro-3- H H H H CR⁵ CR⁶ methyl trifluoromethylphenylmethyl 363 S methyl methyl n-butyl H H H H CR⁵ CR⁶ 364 S methyl methyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 365 S methyl methyl cyclopropylmethyl H H H H CR⁵ CR⁶ 366 S methyl methyl 2-t-butoxyethyl H H H H CR⁵ CR⁶ 367 S methyl methyl 3,4-difluorophenylmethyl H H H H CR⁵ CR⁶ 368 S methyl methyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 369 S methyl methyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 370 S H 3-cyanophenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 371 S methyl 4-(1-hydroxy-1- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ methyl- ethyl)phenyl 372 S methyl 4-(pyridin-4-yloxy)phenyl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 373 S methyl 4-(pyridin-3-yloxy)phenyl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 374 S methyl 4-(1-hydroxy-1- 4-fluoro-3- H H H H CR⁵ CR⁶ methyl-ethyl)phenyl trifluoromethylphenylmethyl 375 S methyl 3-methoxycarbonylphenyl 4-fluoro-3- H F H H CR⁵ CR⁶ trifluoromethylphenylmethyl 376 S methyl 3- 4-fluoro-3- H F H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 377 S methyl 2-methylthio- 4-fluoro-3- H H H H CR⁵ CR⁶ pyridin-3-yl trifluoromethylphenylmethyl 378 S methyl 6-methylthiopyridin- 4-fluoro-3- H H H H CR⁵ CR⁶ 3-yl trifluoromethylphenylmethyl 379 S H pyridin-3-yl 3-methoxycarbonylphenylmethyl H H H H CR⁵ CR⁶ 380 S H pyridin-3-yl 4-methoxycarbonylphenylmethyl H H H H CR⁵ CR⁶ 381 S pyrrolidin- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ 1-ylmethyl trifluoromethylphenylmethyl 382 S H methyl n-butyl H H H H CR⁵ CR⁶ 383 S H pyridin-3-yl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 384 S methyl 2-oxo-2,3- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ dihydro- benzooxazol-6- yl 385 S methylcarbonyl 4- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ carboxyphenyl 386 S methylcarbonyl 4-bromophenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 387 S methylcarbonyl 4-cyanophenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 388 S 1- 4-bromophenyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- trifluoromethylphenylmethyl 1- methyl- ethyl 389 S 1- 4- 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- methylcarbonylphenyl trifluoromethylphenylmethyl 1- methyl- ethyl 390 S bromo 4- ethyl H H H H CR⁵ CR⁶ carboxyphenyl 391 S bromo 4- propyl H H H H CR⁵ CR⁶ carboxyphenyl 392 S bromo 4- pentyl H H H H CR⁵ CR⁶ carboxyphenyl 393 S bromo 4- hexyl H H H H CR⁵ CR⁶ carboxyphenyl 394 S bromo 4- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ carboxyphenyl 395 S bromo 4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ carboxyphenyl 396 S bromo 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ carboxyphenyl 397 S bromo 4- 3-t-butoxypropyl H H H H CR⁵ CR⁶ carboxyphenyl 398 S methyl 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 399 S methyl 4- cyclopropylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 400 S methyl 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ carboxyphenyl 401 S methyl 4- 2-t-butoxyethyl H H H H CR⁵ CR⁶ carboxyphenyl 402 S methyl 4-methoxycarbonylphenyl ethyl H H H H CR⁵ CR⁶ 403 S methyl 4- ethyl H H H H CR⁵ CR⁶ carboxyphenyl 404 S methyl 4- propyl H H H H CR⁵ CR⁶ carboxyphenyl 405 S bromo pyridin-3-yl 3-methoxycarbonylphenylmethyl H H H H CR⁵ CR⁶ 406 S bromo pyridin-3-yl 4-methoxycarbonylphenylmethyl H H H H CR⁵ CR⁶ 407 S bromo pyridin-3-yl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 408 S chloro pyridin-3-yl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 409 S methyl 4- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ carboxyphenyl 410 S methyl 4- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ carboxyphenyl 411 S H 4-cyanophenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 412 S methyl 4-methoxycarbonylphenyl 4,4,4-trifluorobutyl H F H H CR⁵ CR⁶ 413 S H 4- 4-fluoro-3- H H H H CR⁵ CR⁶ aminocarbonylphenyl trifluoromethylphenylmethyl 414 S H 4- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ aminocarbonylphenyl 415 S 1- 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- trifluoromethylphenylmethyl 1- methyl- ethyl 416 S methyl 4-methoxycarbonylphenyl 3-t-butoxypropyl H H H H CR⁵ CR⁶ 417 S methylamino- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ methyl trifluoromethylphenylmethyl 418 S dimethylamino- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ methyl trifluoromethylphenylmethyl 419 S formyl 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ 420 S dimethylamino- 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ methyl 421 S(O₂) H phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 422 S methoxy 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ 423 S methoxy 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 424 S H 4-(1H-tetrazol- 4-fluoro-3- H H H H CR⁵ CR⁶ 5-yl)phenyl trifluoromethylphenylmethyl 425 S H 4-(1H-tetrazol- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 5-yl)phenyl 426 S methyl 4- 4,4,4-trifluorobutyl H F H H CR⁵ CR⁶ carboxyphenyl 427 S methyl 4- 4-fluoro-3- H F H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 428 S bromo 4-(1H-tetrazol- n-butyl H H H H CR⁵ CR⁶ 5-yl)phenyl 429 S bromo 4-(1H-tetrazol- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 5-yl)phenyl 430 S(O₂) H 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ 431 S(O₂) bromo phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 432 S(O₂) H 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 433 S(O₂) bromo 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ 434 S(O₂) methoxy 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 435 S(O₂) bromo 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 436 S(O₂) methoxy 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ 437 S bromo 4- cyclobutylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 438 S bromo 4- cyclopentylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 439 S bromo 4- bicyclo[2.2.1]hept- H H H H CR⁵ CR⁶ carboxyphenyl 2-ylmethyl 440 S bromo 4- tetrahydropyran-4-ylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 441 S bromo 4- 2- H H H H CR⁵ CR⁶ carboxyphenyl (dimethylamino)ethyl 442 S H 4-(5-oxo-4,5- n-butyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 443 S bromo 4-(5-oxo-4,5- n-butyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 444 S H 4- n-butyl H H H H CR⁵ CR⁶ dimethylaminophenyl 445 S H 4-(pyrrolidin-1- n-butyl H H H H CR⁵ CR⁶ yl)phenyl 446 S H 4-(morpholin-4- n-butyl H H H H CR⁵ CR⁶ yl)phenyl 447 S H 4-(1-methyl- n-butyl H H H H CR⁵ CR⁶ piperazin-4-yl)phenyl 448 S methyl 2- n-butyl H H H H CR⁵ CR⁶ dimethylaminopyridin- 3-yl 449 S H 4-(1H-tetrazol- n-butyl H H H H CR⁵ CR⁶ 5-yl)phenyl 450 S methyl 4- n-butyl H F H H CR⁵ CR⁶ carboxyphenyl 451 S H 4- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ carboxyphenyl 452 S bromo 4- isobutyl H H H H CR⁵ CR⁶ carboxyphenyl 453 S bromo 4- 2- H H H H CR⁵ CR⁶ carboxyphenyl (cyclohexyloxy)ethyl 454 S bromo 4- 3-methoxy-3-methyl- H H H H CR⁵ CR⁶ carboxyphenyl butyl 455 S methyl 3-(2H-tetrazol- 4-fluoro-3- H H H H CR⁵ CR⁶ 5-yl)phenyl trifluoromethylphenylmethyl 456 S H 4- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ carboxyphenyl 457 S dimethylamino- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ carbonyl trifluoromethylphenylmethyl 458 S methylamino- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ carbonyl trifluoromethylphenylmethyl 459 S aminocarbonyl phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 460 S(O₂) methylcarbonyl phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 461 S H 3- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dimethylaminosulfonylphenyl 462 S H 3- 4-fluoro-3- H H H H CR⁵ CR⁶ dimethylaminosulfonylphenyl trifluoromethylphenylmethyl 463 S(O₂) 1- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- trifluoromethylphenylmethyl 1- methyl- ethyl 464 S(O₂) 1- phenyl 3,4- H H H H CR⁵ CR⁶ hydroxy- difluorophenylmethyl ethyl 465 S aminocarbonyl 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ 466 S methylamino- 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ carbonyl 467 S dimethylamino- 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ carbonyl 468 S aminocarbonyl 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 469 S dimethylamino- 4- n-butyl H H H H CR⁵ CR⁶ carbonyl carboxyphenyl 470 S H 4-(2-oxo-2,3- n-butyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 471 S H 4-(N-hydroxy- n-butyl H H H H CR⁵ CR⁶ acetamidinyl)phenyl 472 S H 4-(N- n-butyl H H H H CR⁵ CR⁶ (methylcarbonyloxy)- acetamidinyl)phenyl 473 S bromo 4-(N-hydroxy- n-butyl H H H H CR⁵ CR⁶ acetamidinyl)phenyl 474 S bromo 4-(1H-tetrazol- cyclopropylmethyl H H H H CR⁵ CR⁶ 5-yl)phenyl 475 S bromo 4-(1H-tetrazol- 4-fluoro-3- H H H H CR⁵ CR⁶ 5-yl)phenyl trifluoromethylphenylmethyl 476 S H 4-bromophenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 477 S chloro 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 478 S chloro 4- cyclopropylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 479 S chloro 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ carboxyphenyl 480 S chloro 4- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ carboxyphenyl 481 S bromo 4-(5-thioxo-4,5- n-butyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 482 S H 4-(N-hydroxy- 4-fluoro-3- H H H H CR⁵ CR⁶ acetamidinyl)phenyl trifluoromethylphenylmethyl 483 S H 4-(5-oxo-4,5- 4-fluoro-3- H H H H CR⁵ CR⁶ dihydro- trifluoromethylphenylmethyl [1,2,4]oxadiazol- 3-yl)phenyl 484 S bromo 4-(2-oxo-2,3- n-butyl H H H H CR⁵ CR⁶ dihydro-214- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 485 S chloro 4-(2-oxo-2,3- n-butyl H H H H CR⁵ CR⁶ dihydro-214- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 486 S methyl 4- phenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 487 S methyl 4- 4-fluorophenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 488 S methyl 4- 3,4- H H H H CR⁵ CR⁶ carboxyphenyl difluorophenylmethyl 489 S methyl 4- 3-chloro-4- H H H H CR⁵ CR⁶ carboxyphenyl fluorophenylmethyl 490 S methyl 4- 4-difluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 491 S methyl 4- 3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 492 S methyl 4- 4-methanesulfonylphenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 493 S methyl 4- pentafluorophenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 494 S methyl 4- 4-trifluoromethylsulfonylphenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 495 S methyl 4- pyridin-2-ylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 496 S methyl 4- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 497 S methyl 4- 3-fluoro-4- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 498 S H 4-nitrophenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 499 S H 4-aminophenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 500 S methyl- 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ carbonylamino 501 S cyclopentyl 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 502 S cyclopentyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 503 S methylcarbonyl 4-bromophenyl n-butyl H H H H CR⁵ CR⁶ 504 S 1- 4-methoxycarbonylphenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ hydroxy- 1- methyl- ethyl 505 S 1- 4- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ hydroxy- carboxyphenyl 1- methyl- ethyl 506 S 1- 4-bromophenyl n-butyl H H H H CR⁵ CR⁶ hydroxy- 1- methyl- ethyl 507 S H 4-(methanesulfonylamino)phenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 508 S methane- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ sulfonylamino trifluoromethylphenylmethyl 509 S methyl- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ carbonylamino trifluoromethylphenylmethyl 510 S methyl 2-carboxyethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 511 S bromo 4-(5-oxo-4,5- 4-fluoro-3- H H H H CR⁵ CR⁶ dihydro- trifluoromethylphenylmethyl [1,2,4]oxadiazol- 3-yl)phenyl 512 S chloro 4-(5-oxo-4,5- 4-fluoro-3- H H H H CR⁵ CR⁶ dihydro- trifluoromethylphenylmethyl [1,2,4]oxadiazol- 3-yl)phenyl 513 S H 4-(5-oxo-4,5- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 514 S bromo 4-(5-oxo-4,5- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 515 S chloro 4-(5-oxo-4,5- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 516 S 1- 4-methoxycarbonylphenyl n-butyl H H H H CR⁵ CR⁶ hydroxy- 1- methyl- ethyl 517 S methyl 4- 3,4,5- H H H H CR⁵ CR⁶ carboxyphenyl trifluorophenylmethyl 518 S methyl 4- 4- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 519 S methyl 4- 2-fluoro-5- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 520 S methyl 4- 2,5- H H H H CR⁵ CR⁶ carboxyphenyl dichlorophenylmethyl 521 S methyl 4- 4-chloro-3- H H H H CR⁵ CR⁶ carboxyphenyl fluorophenylmethyl 522 S methyl 4- 4-fluoro-2- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 523 S methyl 4- benzo[1,3]dioxol-5-ylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 524 S methyl 4- 2,2-difluoro- H H H H CR⁵ CR⁶ carboxyphenyl benzo[1,3]dioxol-5-ylmethyl 525 S methyl 4- 3,4-dimethoxyphenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 526 S methyl 4- 4-trifluoromethylthiophenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 527 S methyl 4-carboxythien- 4-fluoro-3- H H H H CR⁵ CR⁶ 2-yl trifluoromethylphenylmethyl 528 S methyl 5-carboxy-3- 4-fluoro-3- H H H H CR⁵ CR⁶ methyl-thien-2- trifluoromethylphenylmethyl yl 529 S methyl 5-carboxyfuran- 4-fluoro-3- H H H H CR⁵ CR⁶ 2-yl trifluoromethylphenylmethyl 530 S chloro 4-methoxycarbonylphenyl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 531 S chloro 4-methoxycarbonylphenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 532 S H methylamino n-butyl H H H H CR⁵ CR⁶ 533 S methyl methylamino 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 534 S 1S*- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- trifluoromethylphenylmethyl ethyl 535 S 1R*- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- trifluoromethylphenylmethyl ethyl 536 S(O₂) dimethylamino 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 537 S chloro 4- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ carboxyphenyl 538 S chloro 4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ carboxyphenyl 539 S methyl 4-(1H-tetrazol- n-butyl H H H H CR⁵ CR⁶ 5-yl)phenyl 540 S methyl 4-(2-oxo-2,3- n-butyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 541 S methyl 4-(5-oxo-4,5- n-butyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 542 S methyl 4-(1H-tetrazol- 4-fluoro-3- H H H H CR⁵ CR⁶ 5-yl)phenyl trifluoromethylphenylmethyl 543 S methyl 4-(2-oxo-2,3- 4-fluoro-3- H H H H CR⁵ CR⁶ dihydro-2λ4- trifluoromethylphenylmethyl [1,2,3,5]oxathiadiazol- 4- yl)phenyl 544 S methyl 4-(5-oxo-4,5- 4-fluoro-3- H H H H CR⁵ CR⁶ dihydro- trifluoromethylphenylmethyl [1,2,4]oxadiazol- 3-yl)phenyl 545 S methyl 4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ carboxyphenyl 546 S methyl 3-cyanophenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 547 S isopropyl phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 548 S isopropyl phenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 549 S methyl 3-cyanophenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 550 S methyl 3-cyanophenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 551 S methyl 3-cyanophenyl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 552 S methyl 3-cyanophenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 553 S chloro methylamino n-butyl H H H H CR⁵ CR⁶ 554 S bromo methylamino n-butyl H H H H CR⁵ CR⁶ 555 S methyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ (hydroxyaminocarbonyl)phenyl trifluoromethylphenylmethyl 556 S H 4- n-butyl H H H H CR⁵ CR⁶ carboxyphenyl 557 S methyl 4- 4-fluoro-3- H CF₃ H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 558 S methyl 4- n-butyl H CF₃ H H CR⁵ CR⁶ carboxyphenyl 559 S bromo 4-(morpholin-4- n-butyl H H H H CR⁵ CR⁶ yl)phenyl 560 S bromo 4- n-butyl H H H H CR⁵ CR⁶ dimethylaminophenyl 561 S chloro 4- n-butyl H H H H CR⁵ CR⁶ dimethylaminophenyl 562 S chloro 4-(morpholin-4- n-butyl H H H H CR⁵ CR⁶ yl)phenyl 563 S isopropyl 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 564 S isopropyl 4-methoxycarbonylphenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 565 S isopropyl 4-methoxycarbonylphenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 566 S isopropyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 567 S isopropyl 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ carboxyphenyl 568 S isopropyl 4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ carboxyphenyl 569 S H 4-(1H-tetrazol- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 5-yl)phenyl 570 S methyl 4-(1H-tetrazol- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 5-yl)phenyl 571 S H 4-(1H-tetrazol- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 5-yl)phenyl 572 S methyl 4-(1H-tetrazol- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 5-yl)phenyl 573 S H 3-cyanophenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 574 S H 3-cyanophenyl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 575 S H 3-cyanophenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 576 S bromo 3-(1H-tetrazol- 4-fluoro-3- H H H H CR⁵ CR⁶ 5-yl)phenyl trifluoromethylphenylmethyl 577 S(O₂) bromo phenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 578 S chloro 3-(1H-tetrazol- 4-fluoro-3- H H H H CR⁵ CR⁶ 5-yl)phenyl trifluoromethylphenylmethyl 579 S bromo 4-(1H-tetrazol- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 5-yl)phenyl 580 S chloro 4-(1H-tetrazol- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 5-yl)phenyl 581 S bromo 4-(2-oxo-2,3- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 582 S chloro 4-(2-oxo-2,3- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 583 S bromo 4-(5-oxo-4,5- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 584 S chloro 4-(5-oxo-4,5- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 585 S chloro 4-aminophenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 586 S H 4-amino-3- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ chlorophenyl 587 S bromo 4-aminophenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 588 S bromo 4-amino-3- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ bromophenyl 589 S methyl 4-carboxy-2- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ fluorophenyl 590 S methyl 4-carboxy-2- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ fluorophenyl 591 S methyl 4-carboxy-2- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ fluorophenyl 592 S methyl 4-carboxy-2- 4-fluoro-3- H H H H CR⁵ CR⁶ fluorophenyl trifluoromethylphenylmethyl 593 S methyl 4-carboxy-2- n-butyl H H H H CR⁵ CR⁶ fluorophenyl 594 S bromo 4-(1H-tetrazol- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 5-yl)phenyl 595 S bromo 4-(1H-tetrazol- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 5-yl)phenyl 596 S H 4-(2-oxo-2,3- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 597 S H 4-(5-oxo-4,5- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 598 S methyl 4-(2-oxo-2,3- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4-yl)- phenyl 599 S methyl 4-(5-oxo-4,5- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 600 S methyl 2-(methoxycarbonyl)ethyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 601 S methyl 2-(methoxycarbonyl)ethyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 602 S methyl 2-(methoxycarbonyl)ethyl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 603 S methyl 2-(methoxycarbonyl)ethyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 604 S methyl 2-carboxyethyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 605 S methyl 2-carboxyethyl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 606 S methyl 2-carboxyethyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 607 S bromo 4-(2-oxo-2,3- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 608 S bromo 4-(5-oxo-4,5- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 609 S chloro 4-(5-oxo-4,5- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 610 S H 4-(2-oxo-2,3- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4-yl)- phenyl 611 S methyl 4-(2-oxo-2,3- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 612 S H 4-(5-oxo-4,5- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 613 S methyl 4-(5-oxo-4,5- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 614 S methyl phenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 615 S methyl phenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 616 S methyl phenyl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 617 S methyl phenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 618 S(O₂) methyl phenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 619 S(O₂) methyl phenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 620 S(O₂) methyl phenyl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 621 S(O₂) methyl phenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 622 S(O₂) methyl phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 623 S methyl 4-(methanesulfonylamino- 4-fluoro-3- H H H H CR⁵ CR⁶ carbonyl)phenyl trifluoromethylphenylmethyl 624 S bromo 4-(2-oxo-2,3- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 625 S chloro 4-(2-oxo-2,3- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro-2λ4- [1,2,3,5]oxathiadiazol- 4- yl)phenyl 626 S bromo 4-(5-oxo-4,5- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 627 S chloro 4-(5-oxo-4,5- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 628 S methyl 4-methoxycarbonylphenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 629 S methyl 4- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ methoxycarbonylphenyl 630 S methyl 4-methoxycarbonylphenyl 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ 631 S methyl 4-methoxycarbonylphenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 632 S(O₂) methyl 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ carboxyphenyl 633 S(O₂) methyl 4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ carboxyphenyl 634 S(O₂) methyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 635 S chloro 4-(1H-tetrazol- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 5-yl)phenyl 636 S chloro 4-(1H-tetrazol- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 5-yl)phenyl 637 S methyl 4-(5-oxo-4,5- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]thiadiazol- 3-yl)phenyl 638 S H 4-carboxy-2- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ fluorophenyl 639 S H 4-carboxy-2- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ fluorophenyl 640 S methyl 4-(5-oxo-4,5- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]thiadiazol- 3-yl)phenyl 641 S methyl 4-(5-oxo-4,5- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]thiadiazol- 3-yl)phenyl 642 S H 4-(5-oxo-4,5- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]thiadiazol- 3-yl)phenyl 643 S(O₂) dimethylamino phenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 644 S(O₂) methylamino phenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 645 S(O₂) 4- phenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ methyl- piperazin- 1-yl 646 S(O₂) amino phenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 647 S(O₂) piperazin- phenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 1-yl 648 S(O₂) methylamino phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 649 S(O₂) 4- phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ methyl- trifluoromethylphenylmethyl piperazin- 1-yl 650 S bromo 4-aminophenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 651 S bromo 4-amino-3- 4-fluoro-3- H H H H CR⁵ CR⁶ bromophenyl trifluoromethylphenylmethyl 652 S H 4- 4-fluoro-3- H H H H CR⁵ CR⁶ methanesulfonylaminophenyl trifluoromethylphenylmethyl 653 S H 4-aminophenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 654 S H 4-bromophenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 655 S H 4-bromophenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 656 S 1- 4-bromophenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ hydroxy- 1- methyl- ethyl 657 S 1- 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ hydroxy- carboxyphenyl 1- methyl- ethyl 658 S 1- 4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ hydroxy- carboxyphenyl 1- methyl- ethyl 659 S chloro 4-(methanesulfonylamino)phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 660 S bromo 4-(methanesulfonylamino)phenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 661 S bromo 3-bromo-4- 4-fluoro-3- H H H H CR⁵ CR⁶ (methanesulfonylamino)phenyl trifluoromethylphenylmethyl 662 S methyl trifluoromethyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 663 S H trifluoromethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 664 S methyl trifluoromethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 665 S methyl trifluoromethyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 666 S chloro 4-aminophenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 667 S chloro 4-amino-3- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ chloro-phenyl 668 S bromo 4-aminophenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 669 S methyl 2,2,2- 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoroethyl trifluoromethylphenylmethyl 670 S methyl 2,2,2- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ trifluoroethyl 671 S methyl 2,2,2- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ trifluoroethyl 672 S methyl 2,2,2- 4,4,4-trifluorobutyl H H H H CR⁵ CR⁶ trifluoroethyl 673 S methyl 2,2,2- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ trifluoroethyl 674 S cyclopropyl 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 675 S cyclopropyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 676 S chloro 4-(methanesulfonylamino)phenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 677 S bromo 4-(methanesulfonylamino)phenyl 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ 678 S H 4-(methanesulfonylamino)phenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 679 S chloro 4-(methanesulfonylamino)phenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 680 S bromo 4-(methanesulfonylamino)phenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 681 S chloro 3,5-dichloro-4- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ methanesulfonylaminophenyl 682 S chloro 3,5-dichloro-4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ methanesulfonylaminophenyl 683 S bromo 3-bromo-4- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ (methanesulfonylamino)phenyl 684 S H 4-(5-oxo-4,5- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]thiadiazol- 3-yl)phenyl 685 S H 4-carboxy-2- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ fluorophenyl 686 S H 4-carboxy-2- 4-fluoro-3- H H H H CR⁵ CR⁶ fluorophenyl trifluoromethylphenylmethyl 687 S H 4-(5-oxo-4,5- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]thiadiazol- 3-yl)-phenyl 688 S H 4-methylaminophenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 689 S H 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dimethylaminophenyl 690 S chloro 4-methylaminophenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 691 S chloro 3-chloro-4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ methylaminophenyl 692 S bromo 3-bromo-4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ methylaminophenyl 693 S bromo 4-methylaminophenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 694 S chloro 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ trifluoromethylcarbonyl- aminophenyl 695 S bromo 4- 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylcarbonyl- trifluoromethylphenylmethyl aminophenyl 696 S cyclobutyl 4-methoxycarbonylphenyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 697 S H 2,2,2- 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoroethyl trifluoromethylphenylmethyl 698 S cyclobutyl 4- 4-fluoro-3- H H H H CR⁵ CR⁶ carboxyphenyl trifluoromethylphenylmethyl 699 S methyl 3- 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxypropyl trifluoromethylphenylmethyl 700 S methyl 2-(2,2,2- 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoro-acetyl)- trifluoromethylphenylmethyl 1,2,3,4- tetrahydro- isoquinolin-7-yl 701 S methyl 4-(2- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ dimethylaminomethyl- imidazol-1- yl)phenyl 702 S bromo 2,2,2- 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoroethyl trifluoromethylphenylmethyl 703 S chloro 2,2,2- 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoroethyl trifluoromethylphenylmethyl 704 S hydroxymethyl 2,2,2- 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoroethyl trifluoromethylphenylmethyl 705 S bromo methylamino 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 706 S bromo 4-(5-oxo-4,5- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]thiadiazol- 3-yl)phenyl 707 S bromo 4-carboxy-2- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ fluorophenyl 708 S bromo 4-(5-oxo-4,5- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]thiadiazol- 3-yl)phenyl 709 S bromo 4-carboxy-2- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ fluorophenyl 710 S bromo 4-carboxy-2- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ fluorophenyl 711 S bromo 4-carboxy-2- 4-fluoro-3- H H H H CR⁵ CR⁶ fluorophenyl trifluoromethylphenylmethyl 712 S bromo 4-(5-oxo-4,5- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]thiadiazol- 3-yl)phenyl 713 S H 3- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ methanesulfonylaminophenyl 714 S chloro 3- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ methanesulfonylaminophenyl 715 S bromo 3- 3,3,3-trifluoropropyl H H H H CR⁵ CR⁶ methanesulfonylaminophenyl 716 S chloro 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ methanesulfonylaminophenyl 717 S bromo 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ methanesulfonylaminophenyl 718 S chloro 4-(cyclopropylsulfonyl- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ amino)phenyl 719 S bromo 4-(cyclopropylsulfonyl- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ amino)phenyl 720 S methyl benzimidazol-2- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ yl 721 S methyl quinoxalin-5-yl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 722 S methyl 1-methyl- 4-fluoro-3- H H H H CR⁵ CR⁶ benzimidazol-2- trifluoromethylphenylmethyl yl 723 S methyl quinoxalin-5-yl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 724 S methyl 2-formylethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 725 S methyl 3-hydroxy-3- 4-fluoro-3- H H H H CR⁵ CR⁶ methyl-butyl trifluoromethylphenylmethyl 726 S methyl benzimidazol-2- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ yl 727 S methyl 5-chloro-1- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ methyl- benzimidazol-2- yl 728 S methyl benzimidazol-2- 4-fluoro-3- H H H H CR⁵ CR⁶ yl trifluoromethylphenylmethyl 729 S methyl benzimidazol-2- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ yl 730 S methylcarbonyl 4-bromophenyl 4-fluorophenylmethyl H H H H CR⁵ CR⁶ 731 S methylcarbonyl 4-bromophenyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 732 S methylcarbonyl 4-bromophenyl phenylmethyl H H H H CR⁵ CR⁶ 733 S methylcarbonyl 4-bromophenyl 3-chloro-4- H H H H CR⁵ CR⁶ fluorophenylmethyl 734 S 1- 4-bromophenyl 4-fluorophenylmethyl H H H H CR⁵ CR⁶ hydroxy- 1- methyl- ethyl 735 S 1- 4-bromophenyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ hydroxy- 1- methyl- ethyl 736 S 1- 4-bromophenyl phenylmethyl H H H H CR⁵ CR⁶ hydroxy- 1- methyl- ethyl 737 S 1- 4-bromophenyl 3-chloro-4- H H H H CR⁵ CR⁶ hydroxy- fluorophenylmethyl 1- methyl- ethyl 738 S methyl 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dimethylaminophenyl 739 S methyl 4-diethylaminophenyl 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 740 S methyl 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ (thiomorpholin- 4-yl)phenyl 741 S methyl 4-(morpholin-4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ yl)phenyl 742 S methyl 4-(piperazin-1- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ yl)phenyl 743 S H 4- 4-fluoro-3- H H H H CR⁵ CR⁶ methanesulfonylamino)- trifluoromethylphenylmethyl 2- methoxyphenyl 744 S chloro 4- 4-fluoro-3- H H H H CR⁵ CR⁶ methanesulfonylamino- trifluoromethylphenylmethyl 2- methoxyphenyl 745 S methyl 1-methyl- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ benzimidazol-2- yl 746 S methyl 1-methyl- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ benzimidazol-2- yl 747 S methyl 2-amino- 4-fluoro-3- H H H H CR⁵ CR⁶ indan-5-yl trifluoromethylphenylmethyl 748 S methyl 4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ dimethylaminophenyl 749 S methyl 4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ (thiomorpholin- 4-yl)phenyl 750 S methyl 4-(morpholin-4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ yl)phenyl 751 S methyl 4-(piperidin-1- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ yl)phenyl 752 S methyl 4-(piperidin-1- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ yl)phenyl 753 S cyclopropyl 4-methoxycarbonylphenyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 754 S cyclobutyl 4-methoxycarbonylphenyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 755 S cyclopropyl 4- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 756 S cyclobutyl 4- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ carboxyphenyl 757 S methyl 3-(methoxycarbonyl)propyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 758 S methyl 4-hydroxybutyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 759 S methyl 4-hydroxy-4- 4-fluoro-3- H H H H CR⁵ CR⁶ methylpentyl trifluoromethylphenylmethyl 760 S methyl 2-(methoxycarbonyl)ethyl 3-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 761 S methyl methoxycarbonylmethyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 762 S methyl 2-carboxyethyl 3-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 763 S methyl 3-hydroxy-3- 3-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ methyl-butyl 764 S methyl 3- 3-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ hydroxypropyl 765 S methyl 3-carboxypropyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 766 S chloro 5-chloro-2- 4-fluoro-3- H H H H CR⁵ CR⁶ methoxy-4- trifluoromethylphenylmethyl (methanesulfonylamino)phenyl 767 S methyl 2-methyl- 4-fluoro-3- H H H H CR⁵ CR⁶ 1,2,3,4- trifluoromethylphenylmethyl tetrahydro- isoquinolin-7-yl 768 S isopropenyl ethyl 4-chloro-2-fluoro-5- H H H H CR⁵ CR⁶ methoxyphenylmethyl 769 S methyl 3-bromopropyl 3-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 770 S methyl cyclopropyl 3-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 771 S methyl 4-bromobutyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 772 S methylcarbonyl 4-cyanophenyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 773 S methylcarbonyl 4-cyanophenyl 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 774 S methyl 4-carboxy-3- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ fluorophenyl 775 S methyl 4-carboxy-3- 4-fluoro-3- H H H H CR⁵ CR⁶ fluorophenyl trifluoromethylphenylmethyl 776 S 1- ethyl 2-fluoro-3-methoxyphenylmethyl H H H H CR⁵ CR⁶ hydroxy- 1- methyl- ethyl 777 S methyl 4-(4-methyl- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ piperazin-1-ylcarbonyl)phenyl 778 S methyl 3-(imidazol-1- 3-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ yl)propyl 779 S methyl 4-(imidazol-1- 4-fluoro-3- H H H H CR⁵ CR⁶ yl)butyl trifluoromethylphenylmethyl 780 S chloro 2-hydroxy-4- 4-fluoro-3- H H H H CR⁵ CR⁶ (methanesulfonylamino)phenyl trifluoromethylphenylmethyl 781 S 1- 4- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ hydroxy- carboxyphenyl 1- methyl- ethyl 782 S methyl 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ (pyrrolidin-3S- ylaminocarbonyl)- phenyl 783 S methyl 4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ (pyrrolidin-3R- ylaminocarbonyl)- phenyl 784 S methyl 4-(5-oxo-4,5- 4-fluoro-3- H H H H CR⁵ CR⁶ dihydro- trifluoromethylphenylmethyl [1,2,4]thiadiazol- 3-yl)phenyl 785 S methyl 4-(1H-tetrazol- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 5-yl)phenyl 786 S methyl 6- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dimethylamino- pyridin-3-yl 787 S methyl 6- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ (dimethylamino)pyridin- 3-yl 788 S methyl 6-(morpholin-4- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ yl)pyridin-3-yl 789 S methyl 6- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ (dimethylamino)pyridin- 3-yl 790 S methyl 6-(morpholin-4- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ yl)pyridin-3-yl 791 S methyl methoxycarbonylmethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 792 S methyl carboxymethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 793 S methyl 2-hydroxyethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 794 S methyl 2-methoxycarbonylethyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 795 S methyl 2-carboxyethyl 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 796 S methyl 3-hydroxy-3- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ methyl-butyl 797 S methyl 2-bromoethyl 4-fluoro-3- H H H H CR⁵ CR⁶ trifluoromethylphenylmethyl 798 S methyl 6-(morpholin-4- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ yl)pyridin-3-yl 799 S methyl 4- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ dimethylaminophenyl 800 S methyl 4-(morpholin-4- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ yl)phenyl 801 S methyl 4-(5-oxo-4,5- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)phenyl 802 S 1- ethyl 2,4,5-trifluoro-3- H H H H CR⁵ CR⁶ hydroxy- methoxyphenylmethyl 1- methyl- ethyl 803 S isopropenyl ethyl 2,4,5-trifluoro-3- H H H H CR⁵ CR⁶ methoxyphenylmethyl 804 S methyl 6-(1H-tetrazol- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ 5-yl)pyridin-3- yl 805 S methyl 6-(1H-tetrazol- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ 5-yl)pyridin-3- yl 806 S methyl 6-(1H-tetrazol- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ 5-yl)pyridin-3- yl 807 S methyl 6-(5-oxo-4,5- 2-(cyclopropyl)ethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)pyridin-3- yl 808 S methyl 6-(5-oxo-4,5- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)pyridin-3- yl 809 S methyl 6-(5-oxo-4,5- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]oxadiazol- 3-yl)pyridin-3- yl 810 S methyl 4-(5-oxo-4,5- 4-trifluoromethoxyphenylmethyl H H H H CR⁵ CR⁶ dihydro- [1,2,4]thiadiazol- 3-yl)phenyl 811 S methyl 4-(5-oxo-4,5- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ dihydro-1H- [1,2,4]triazol-3- yl)phenyl 812 S methyl 4-(1-methyl-5- 5,5,5-trifluoropentyl H H H H CR⁵ CR⁶ oxo-4,5- dihydro-1H- [1,2,4]triazol-3- yl)phenyl 813 S chloro phenyl 4-fluoro-3- H H H NA CR⁵ N trifluoromethylphenylmethyl 814 S chloro 3- 4-fluoro-3- H H H NA CR⁵ N carboxyphenyl trifluoromethylphenylmethyl 815 S chloro 4- 3,3,3-trifluoropropyl H H H NA CR⁵ N carboxyphenyl 816 S chloro 3-methoxycarbonylphenyl 4-fluoro-3- H H H NA CR⁵ N trifluoromethylphenylmethyl 817 S H phenyl 3-fluoropropyl H H H H CR⁵ CR⁶ 818 S methyl phenyl 2-fluoroethyl H H H H CR⁵ CR⁶ 819 S methyl phenyl 3-fluoropropyl H H H H CR⁵ CR⁶ 820 S hydroxymethyl phenyl 3-fluoropropyl H H H H CR⁵ CR⁶ 821 S 1- phenyl 3-fluoropropyl H H H H CR⁵ CR⁶ hydroxy- ethyl 822 S 1- phenyl 3-fluoropropyl H H H H CR⁵ CR⁶ methoxy- ethyl 823 S methyl 4-methoxycarbonylphenyl 3-fluoropropyl H H H H CR⁵ CR⁶ 824 S methyl 4- 3-fluoropropyl H H H H CR⁵ CR⁶ carboxyphenyl 825 S methyl 3,4- phenylmethyl H H H H CR⁵ CR⁶ difluorophenyl 826 S methyl 3,4- 4-fluorophenylmethyl H H H H CR⁵ CR⁶ difluorophenyl 827 S 1- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- methoxyphenylmethyl ethyl 828 S H ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ methoxyphenylmethyl 829 S methyl ethyl 2-fluoropyridin-4-ylmethyl H H H H CR⁵ CR⁶ 830 S 1- phenyl 3-fluoropropyl H H H H CR⁵ CR⁶ hydroxy- 1- methyl- ethyl 831 S methyl 3,4- 3-fluoropropyl H H H H CR⁵ CR⁶ difluorophenyl 832 S methoxymethyl phenyl 3-fluoropropyl H H H H CR⁵ CR⁶ 833 S methylcarbonyl phenyl 3-fluoropropyl H H H H CR⁵ CR⁶ 834 S hydroxymethyl 2,5- 3,4- H H H H CR⁵ CR⁶ dibromophenyl difluorophenylmethyl 835 S 1- ethyl 2-fluoro- H H H H CR⁵ CR⁶ hydroxy- pyridin-4-ylmethyl ethyl 836 S 1- ethyl 2-fluoropyridin- H H H H CR⁵ CR⁶ hydroxy- 4-ylmethyl 1- methyl- ethyl 837 S methylcarbonyl ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ methoxyphenylmethyl 838 S 1- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ hydroxy- methoxyphenylmethyl 1- methyl- ethyl 839 S 1- ethyl 4-fluoro-3- H H H H CR⁵ CR⁶ methoxy- trifluoromethylphenylmethyl ethyl 840 S methyl ethyl 2,3,5-trifluoro- H H H H CR⁵ CR⁶ pyridin-4-ylmethyl 841 S methyl 3,4- 2-fluoroethyl H H H H CR⁵ CR⁶ difluorophenyl 842 S H 4-methoxycarbonylphenyl 3-fluoropropyl H H H H CR⁵ CR⁶ 843 S H 4-methoxycarbonylphenyl 2-fluoroethyl H H H H CR⁵ CR⁶ 844 S H phenyl 2-fluoroethyl H H H H CR⁵ CR⁶ 845 S methyl 3-fluoro-4-(4- 4-fluorophenylmethyl H H H H CR⁵ CR⁶ fluorophenylmethoxy)phenyl 846 S methyl 3-fluoro-4- phenylmethyl H H H H CR⁵ CR⁶ (phenylmethoxy)phenyl 847 S H ethyl 2-fluoropyridin-4-ylmethyl H H H H CR⁵ CR⁶ 848 S methylcarbonyl ethyl 2-fluoropyridin-4-ylmethyl H H H H CR⁵ CR⁶ 849 S bromo n-butylamino n-butyl H H H H CR⁵ CR⁶ 850 S H n-butylamino n-butyl H H H H CR⁵ CR⁶

BIOLOGICAL EXAMPLES Example 1a In Vitro Canine TRPM8 Functional Assay

The functional activity of compounds of the formula (I) was determined by measuring changes in intracellular calcium concentration using a Ca²⁺-sensitive fluorescent dye. The changes in fluorescent signal were monitored by a fluorescence plate reader, either a FLIPR™ (Molecular Devices) or FDSS (Hamamatsu). Increases in intracellular Ca²⁺ concentration were readily detected upon activation with icilin.

At 24 hrs prior to assay, HEK293 cells stably expressing canine TRPM8 were seeded in culture medium in black wall, clear-base poly-D-lysine coated 384-well plates (BD Biosciences, NJ, USA) and grown overnight in 5% CO₂ at 37° C. On assay day, growth media was removed and cells were loaded with Calcium 3 Dye (Molecular Devices) for 35 min at 37° C., under 5% CO₂ and then for 25 min at room temperature and atmosphere. Subsequently, cells were tested for agonist-induced increases in intracellular Ca²⁺ levels using FLIPR™ or FDSS. Cells were challenged with a compound of the Formula (I) (at varying concentrations) and intracellular Ca²⁺ was measured for 5 min prior to the addition of icilin to all wells to achieve a final concentration that produces approximately an 80% maximal response. EC₅₀ or IC₅₀ values for compounds of the present invention were determined from eight-point dose-response studies. Curves were generated using the average of quadruplicate wells for each data point. The resultant data are displayed in Table 2.

TABLE 2 % Inh % Inh Cpd IC₅₀ @ 0.2 @ 0.5 No. (μM) (μM) (μM) 1 0.0240 100 2 0.0163* 99 3 0.0350 98 4 0.0040 97 5 0.0630 97 6 0.0113* 99 7 0.0073* 97 8 0.0100 99 9 0.0470 98 10 0.2290 89 11 0.0330 97 12 0.0060 97 13 0.0030 97 14 0.0189* 99 15 0.0050 96 16 0.0060 99 17 0.0220 97 18 0.0810 94 19 58 20 0.0060 98 21 0.0150 98 22 0.0320 98 23 0.0260 99 24 0.0088* 100 25 0.0210 99 26 0.0200 98 27 0.0200 99 28 0.0320 100 29 0.0330 99 30 0.0120 100 31 0.0220 100 32 0.0370 100 33 0.0574 100 34 0.1841 98 35 0.0608 100 36 0.0771 98 37 0.0983 96 38 0.0030 97 39 0.0039 101 40 0.0137 97 41 0.0054 99 42 0.0106 100 43 0.0250 94 44 0.0070 98 45 0.0520 97 46 0.0840 99 47 0.1120 97 48 0.0790 98 49 0.1700 90 50 0.0660 99 51 0.0780 98 52 0.1160 99 53 0.1640 97 54 65 55 0.0655 99 56 0.1031 99 57 0.1080 100 58 0.0455* 98 59 0.0445 98 60 0.0283 97 61 0.0524 95 62 0.0581 98 63 0.0740 98 64 0.0190 96 65 0.0170 97 66 0.0040 96 67 0.0550 77 68 0.0020 99 69 0.0030 96 70 0.0070 99 71 0.0180 98 72 0.0260 99 73 24 74 0.0210 97 75 0.0180 98 76 0.0210 95 77 0.0220 97 78 0.0225 102 79 69 80 0.0290 98 81 0.0150 99 82 0.3190 87 83 0.0480 101 84 0.0350 100 85 0.0240 100 86 0.0530 101 87 0.1700 94 88 0.2610 88 89 0.2050 96 90 0.0210 99 91 33 92 0.0682 79 93 0.0110 98 94 0.0180 98 95 0.0060 97 96 0.0040 98 97 0.0140 96 98 0.0150 97 99 0.0180 99 100 0.0068 103 101 0.0305 101 102 0.0402 98 103 0.0908 80 104 0.0089 98 105 20 106 0.0190 93 107 72 108 71 109 14 110 0.0072 97 111 0.0920 68 112 0.0302 95 113 19 114 0.0511* 93 115 0.0795 95 116 0.1017 98 117 0.0537 99 118 0.0480 100 119 0.1336 93 120 0.1560 75 121 0.0350 86 122 23 123 60 124 14 125 0.0050* 99 126 45 127 0.0080 98 128 0.0090 99 129 0.0028* 101 130 0.1040 98 131 0.0480 95 132 56 133 0.0600 97 134 30 135 18 136 40 137 0.0080 98 138 0.0130 83 139 0.0620 91 140 0.0020 98 141 18 142 60 143 48 144 62 145 0.0141 100 146 0.0480 97 147 0.0782 96 148 0.0021* 98 149 0.0071* 102 101 150 0.0154 100 151 0.0167 96 152 0.0026 95 153 0.0188 97 154 0.0362 96 155 0.0040 99 156 65 157 0.0140 100 158 0.0104 94 159 0.0134 98 160 0.0358 97 161 0.0554 95 162 0.0045 101 163 0.0639 92 164 0.0319 97 165 0.0037 98 166 0.0114 94 167 0.0104 101 168 0.0142 96 169 0.0214 98 170 0.0445 97 171 0.0193 100 172 0.0111 98 173 0.0084 99 174 0.0025 99 175 0.0046 97 176 0.0028 97 177 0.0057 96 178 0.0355 96 179 0.0036 98 180 0.0430 96 181 0.0840 95 182 0.0100 99 183 0.0140 99 184 0.0039 97 185 0.0064 102 186 0.0037 103 187 0.0060 100 188 0.0122* 99 101 189 0.0116 100 190 0.0152 101 191 0.0060 105 192 0.0600 82 193 0.0145 101 194 45 195 0.0473 88 196 0.0080 99 197 0.0070 99 198 0.0100 95 199 0.0130 91 200 29 201 14 202 32 203 0.0150 93 204 0.0060 96 205 0.0030 96 206 0.0130 98 207 0.0160 98 208 0.0120 96 209 0.0320 98 210 0.0080 91 211 0.0300 80 212 0.0114 101 213 0.0014 95 214 0.0021 97 215 0.0060 101 216 0.0140 100 217 0.0030 88 218 0.0010 90 219 0.0078 101 220 0.0012* 98 99 221 0.0050 92 222 0.0017 95 223 0.0023 96 224 0.0010 100 225 0.0040 98 226 0.0020 99 227 0.0006* 101 228 0.0060 101 229 0.0210 99 230 0.0129 100 231 0.0290 95 232 0.0740 94 233 0.0220 93 234 0.0100 93 235 51 236 68 237 0.0248* 87 92 238 0.0930 96 239 0.0920 96 240 43 241 0.1060 97 242 0.0382 95 243 0.0380 98 244 0.0122 100 245 0.0142 102 246 0.0088 102 247 0.0255 99 248 0.0083 98 249 0.0009 97 250 0.0127 102 251 0.0387 95 252 0.0171 102 253 0.0273 101 254 0.1250 58 255 0.0860 89 256 0.0300 87 257 62 258 25 259 24 260 0.0500 86 261 0.0126 97 262 0.0670 94 263 0.2030 52 264 0.0341 99 265 0.0220 90 266 0.0390 86 267 0.0100 96 268 67 269 0.0160 94 270 0.3380 75 271 0.0117* 98 272 0.0062* 97 273 0.0180* 96 274 0.0360 94 275 0.0030* 97 276 0.0710 76 277 0.0390 91 278 0.0010* 98 279 0.0013 97 280 0.0380 87 281 62 282 0.0700 86 283 0.0920 82 284 15 285 0.0025 100 286 0.0070 99 287 0.0298 96 288 0.0200 90 289 0.0270 92 290 0.0053 103 291 0.0058 101 292 0.0008* 98 100 293 0.0078* 101 101 294 0.0018 99 295 0.0330 81 296 0.0020 96 297 21 298 18 299 0.0030 90 300 21 301 63 302 50 303 56 304 29 305 0.0120 97 306 0.0008 102 307 0.0151 101 308 0.0698 92 309 0.0550 93 310 69 311 0.1480 82 312 0.0110 102 313 0.0210 102 314 0.0100 102 315 0.0640 99 316 0.0100 101 317 0.0170 102 318 0.0150 101 319 0.0240 100 320 0.0100 100 321 0.0700 81 322 0.0100 99 323 0.0100 102 324 0.0150 100 325 0.0050 102 326 14 327 0.0370 97 328 0.0350 94 329 17 330 0.0880 80 331 0.0900 71 332 0.0070 100 333 0.0090 101 334 0.0060 98 335 0.0010 101 336 0.0150 101 337 0.0190 101 338 0.0290 95 339 0.0262 94 340 52 341 0.0140 96 342 0.0130 100 343 0.0190 98 344 0.0127 99 345 0.0265 99 346 0.0438 95 347 0.0571 95 348 60 349 42 350 48 351 0.0212 97 352 0.0086 96 353 0.0094 98 354 0.1064 87 355 0.0296 92 356 0.0416 93 357 0.0190 95 358 0.0120 92 359 0.0170 93 360 0.0410 92 361 0.0008 93 362 67 363 0.0510 84 364 0.0440 77 365 38 366 0.0400 85 367 0.0100 91 368 0.0180 96 369 0.0180 98 370 29 371 0.0090 94 372 0.0270 91 373 0.1230 77 374 0.0040 89 375 0.0370 79 376 0.0260 85 377 65 378 0.0970 85 379 54 380 24 381 20 382 17 383 49 384 0.0170 96 385 54 386 0.0128 100.87 387 0.0310 98 388 0.0190 97 389 0.0100 97 390 69 391 0.0470 93 392 0.0070 93 393 0.0050 95 394 0.0090 101 395 0.0030 101 396 0.0050 101 397 0.0080 95 398 0.0060 101 399 0.0360 93 400 0.0050 102 401 0.0050 91 402 38 403 52 404 0.0530 96 405 0.0360 95 406 66 407 0.0430 96 408 0.1220 78 409 0.0100 101 410 0.0170 96 411 43 412 13 413 0.0460 93 414 33 415 0.0050 92 416 0.0120 95 417 0.0620 93 418 0.0690 90 419 0.3450 74 420 48 421 0.0640 90 422 0.0180 97 423 0.0070 93 424 0.0070 95 425 0.0790 86 426 0.0300 95 427 0.0050 95 428 0.0100 93 429 0.0170 93 430 52 431 0.0200 88 432 42 433 0.0330 93 434 0.0170 90 435 0.0330 95 436 0.0040 89 437 0.0090 92 438 0.0020 90 439 0.0020 86 440 0.0140 84 441 37 442 0.0670 81 443 0.0140 94 444 0.1220 92 445 58 446 0.0960 82 447 19 448 0.0120 102 449 0.0880 97 450 0.0290 101 451 0.0680 97 452 0.0180 101 453 0.0020 101 454 0.0040 101 455 0.0360 101 456 67 457 0.0470 93 458 0.0120 102 459 0.0090 102 460 0.0080 102 461 30 462 22 463 0.0260 101 464 0.0070 102 465 0.0630 90 466 66 467 0.0200 100 468 16 469 13 470 15 471 0.0590 97 472 0.0400 88 473 0.0090 102 474 0.0080 101 475 0.0020 102 476 39 477 0.0120 100 478 0.0250 99 479 0.0080 100 480 0.0130 100 481 69 482 0.0240 100 483 0.0090 101 484 0.0210 100 485 0.0210 96 486 0.0040 100 487 0.0020 101 488 0.0010 101 489 0.0006 101 490 0.0010 101 491 0.0010 101 492 0.0620 91 493 0.0008 101 494 0.0009 101 495 0.0550 98 496 0.0008 101 497 0.0004 101 498 41 499 0.0150 101 500 15 501 31 502 0.0100 100 503 0.0470 96 504 0.0180 101 505 0.0240 98 506 0.0310 100 507 0.0340 92 508 47 509 0.0320 100 510 0.0110 102 511 0.0030 101 512 0.0040 102 513 0.0210 101 514 0.0460 100 515 49 516 0.0190 102 517 0.0020 102 518 0.0007 101 519 0.0060 102 520 0.0090 102 521 0.0020 101 522 0.0040 101 523 0.0020 101 524 0.0020 102 525 0.0060 101 526 0.0010 102 527 0.0050 101 528 0.0160 102 529 35 530 54 531 0.0460 88 532 19 533 0.0320 102 534 0.0020 102 535 0.0010 102 536 0.0770 89 537 0.0082 104.64 538 0.0049 104.55 539 0.0067 104.91 540 0.0122 104.6 541 0.0108 104.57 542 0.0023 104.93 543 0.0072 104.46 544 0.0018 105.04 545 0.0019 104.78 546 0.0683 85.683 547 0.0074 104.86 548 0.0289 102.47 549 0.0159 103.68 550 0.0188 103.79 551 0.0886 94.385 552 0.0251 101.3 553 38.688 554 52.301 555 0.0219 102.49 556 0.0482 99.314 557 39.483 558 0.0994 80.935 559 0.0032 104.59 560 0.0657 104.01 561 0.0284 103.38 562 0.0331 102.74 563 0.0493 94.006 564 57.717 565 0.1170 74.399 566 0.0018 104.33 567 0.0103 104.13 568 0.0024 103.99 569 0.0350 88 570 0.0066 101 571 14 572 0.0166 101 573 28 574 16 575 15 576 0.0191 100 577 0.0078 101 578 0.0267 91 579 0.0088 102 580 0.0221 101 581 0.0251 100 582 0.0503 96 583 0.0079 100 584 0.0159 100 585 0.0064 101 586 0.0346 100 587 0.0039 100 588 0.0121 101 589 0.0042 100 590 0.0061 101 591 0.0042 101 592 0.0018 101 593 0.0076 101 594 0.0060 101 595 0.0190 101 596 17 597 25 598 0.0307 101 599 0.0161 101 600 0.0089 101 601 0.0241 100 602 0.0221 101 603 0.0103 101 604 13 605 18 606 0.0905 75 607 0.0368 101 608 0.0181 101 609 0.0537 99 610 55 611 0.0146 101 612 0.0537 97 613 0.0066 101 614 0.0074 101 615 0.0073 101 616 0.0128 101 617 0.0074 101 618 0.0104 101 619 0.0398 101 620 0.0234 101 621 0.0110 101 622 0.0313 89 623 0.0070 101 624 0.0134 103 625 0.0204 103 626 0.0074 103 627 0.0086 103 628 0.0233 103 629 0.0262 103 630 0.0356 103 631 0.0263 103 632 12 633 17 634 55 635 0.0074 101 636 0.0460 103 637 0.0122 104 638 0.0600 100 639 0.1280 84 640 0.0110 103 641 0.0140 103 642 0.0410 90 643 0.0050 103 644 63 645 20 646 55 647 21 648 62 649 26 650 0.0040 102 651 0.0060 103 652 0.0850 102 653 0.0130 102 654 56 655 55 656 0.0537 98 657 0.0075 101 658 0.0043 101 659 0.0141 100 660 0.0112 100 661 0.0141 100 662 50.122 663 17.113 664 53.117 665 27.939 666 0.0081 102.6 667 0.0301 102.96 668 0.0050 102.88 669 0.0512 96.422 670 0.0390 99.074 671 0.0345 100.03 672 0.0749 75.3 673 0.0738 94.378 674 0.0776 85.377 675 0.0024 100 676 0.0259 102.32 677 0.0246 101.48 678 60.964 679 0.0579 100.43 680 0.0561 96.235 681 0.0674 93.318 682 0.0317 101.01 683 0.0258 100.57 684 0.1448 73.142 685 0.0119 102.25 686 0.0047 104.94 687 0.0569 74.496 688 0.0602 99 689 0.0528 86 690 0.0161 101.25 691 0.0160 101.81 692 0.0072 101.48 693 0.0252 103.39 694 42 695 0.0170 101 696 0.0230 97 697 0.0640 92 698 0.0020 102 699 0.0060 103 700 37 701 0.0325 95 702 0.0230 99 703 0.0510 80 704 0.0150 102 705 0.0190 101 706 0.0140 102 707 0.0030 102 708 0.0130 102 709 0.0060 102 710 0.0070 102 711 0.0020 102 712 0.0040 102 713 47 714 0.0290 96 715 0.0240 101 716 0.0090 101 717 0.0050 102 718 0.0390 96 719 0.0230 100 720 52 721 0.0042 102 722 28 723 0.0180 102 724 0.0053 102 725 0.0078 102 726 0.0903 69 727 16 728 44 729 0.0962 75 730 0.0236 100 731 0.0444 87 732 0.0133 100 733 0.0134 100 734 0.0097 102 735 0.0268 101 736 0.0172 101 737 0.0299 101 738 0.0089 102 739 0.0232 90 740 57 741 0.0173 101 742 66 743 32 744 0.0573 99 745 0.0849 74 746 31 747 48 748 0.0053 101 749 64 750 0.0092 101 751 54 752 65 753 0.0272 69 754 0.0164 82 755 0.0009 101 756 0.0014 101 757 0.0108 101 758 0.0051 101 759 0.0183 101 760 0.0459 94 761 0.0400 79 762 0.0253 101 763 0.0277 102 764 0.0221 101 765 0.0136 101 766 0.0078 101 767 0.0892 77 768 0.0188 93 769 0.0440 85 770 0.0072 95 771 0.0072 96 772 0.0057 95 773 0.0167 94 774 0.0013 95 775 0.0016 95 776 0.0067 95 777 56 778 0.1069 87 779 0.0487 79 780 0.1450 72 781 0.0030 102 782 33 783 38 784 0.0033 102 785 0.0022 102 786 0.0154 102 787 0.0149 102 788 0.0259 100 789 0.0117 102 790 0.0220 101 791 0.0231 95 792 23 793 0.0155 102 794 0.0294 101 795 0.0246 100 796 0.0242 101 797 0.0048 102 798 0.0359 102 799 0.0039 102 800 0.0068 102 801 0.0028 102 802 0.0080 101 803 0.0308 101 804 0.0111 102 805 0.0022 103 806 0.0130 102 807 0.0060 103 808 0.0007 102 809 0.0069 103 810 0.0010 102 811 0.0037 103 812 0.0076 103 813 0.0280 90 814 0.1380 80 815 44 816 15 817 0.0730 80 818 0.0620 92 819 0.0210 98 820 0.0280 102 821 0.0090 102 822 0.0490 97 823 0.0220 102 824 0.0380 98 825 0.0250 89 826 0.0240 97 827 0.0066 101 828 0.0427 88 829 0.0230 100 830 0.0150 102 831 0.0500 91 832 0.0880 76 833 0.0130 102 834 0.1230 87 835 0.0551 89 836 0.0240 96 837 0.0150 103 838 0.0041 101 839 0.0159 101 840 0.0981 71.105 841 55 842 63 843 31 844 31 845 24 846 28 847 33 848 68 849 25 850 28 *IC₅₀ values are listed as an average of two or more determinations

Example 1b In Vitro Rat and Human TRPM8 Functional Assay

HEK293 cells are routinely grown as monolayer in Dulbecco's minimum essential medium supplemented with 10% FBS, 1 mM L-glutamine, 100 units/mL penicillin and 100 ug/mL streptomycin. Cells are maintained in 5% CO2 at 37° C.

For functional expression of TRPM8, the full-length cDNA encoding human and rat TRPM8 are subcloned into pCI-NEO mammalian expression vectors. The expression constructs are transiently transfected into HEK293 cells according to the FuGENE 6 transfection Reagent® (ROCHE) instructions. Within twenty-four hours, transiently trasfected cells are harvested and either seeded directly into assay plate or cryopreserved for future usage.

Transfected cells may be either cryopreserved or freshly transfected and plated into clearbase poly-D-lysine coated 384-well plates (BD Biosciences, NJ, USA) at a density of 10,000 cells per well in culture medium and grown overnight. The following day, all medium is removed and the cells are incubated with 52 μL of 0.5×Calcium 3 Dye (Molecular Devices) prepared in complete assay buffer containing 20 mM HEPES, 0.1% BSA, and 2.5 mM probenecid at 37° C. for thirty five minutes. The cells are then incubated for an additional fifteen minutes at room temperature before initiating experiments. Following incubation, plates are inserted into a FDSS instrument, where cells were challenged with compounds of the formula (I) (at varying concentrations) and intracellular Ca2+ are measured for 5 min prior to the addition of icilin at the EC₈₀ concentration. IC50 values for compounds of the formula (I) are determined from eight point dose-response studies.

Maximal fluorescence intensity (FI) achieved upon addition of icilin is exported from the FDSS and further analyzed using GraphPad Prism 3.02 (Graph Pad Software Inc., CA, U.S.A.) where data is normalized to percent of maximal response. The dose response curves from the average of quadruplicate wells for each data point are analyzed by using nonlinear regression of either sigmoidal dose response or sigmoidal dose response (variable slope). Finally, the IC50 values are calculated with the best-fit dose curve determined by Prism. Results are shown in Table 3.

TABLE 3 Cpd Cell rTRPM8 hTRPM8 No preparation IC₅₀, nM IC₅₀, nM 306 Freshly 5.0 4.0 transfected 496 Cryopreserved 1.8 1.4

Example 2 TRPM8 Patch Clamp Assays

For patch clamp experiments, HEK293 cells are stably transfected with canine TRPM8 and cultured in DMEM supplemented with 10% fetal bovine serum, 100 units/ml penicillin, 100 μg/ml streptomycin and 1 mg/ml G418. Cells are maintained at 37° C. and in 5% CO₂.

The extracellular solution contains (in mM): NaCl, 132; EGTA, 1; KCl, 5.4; MgCl₂, 0.8; HEPES, 10; glucose, 10; pH=7.4. Recordings are performed using the conventional whole-cell patch clamp technique, 1-2 days after plating cells onto glass coverslips at densities appropriate for single cell recording. Currents are amplified by a patch clamp amplifier and filtered at 2 kHz (Axopatch 200B, Molecular Devices, Union City, Calif.). Menthol (100 μM) is applied to the cell at 0.5 ml/min via a gravity-fed perfusion system. Recordings involving menthol activation are performed at 22° C.

In experiments where temperatures are varied, temperature ramps are generated by cooling the perfusate in an in-line cooler (Model SC-20, Warner Instruments, Hamden, Conn.) controlled by a temperature controller (Model CL-100, Warner Instruments). The temperature in the vicinity of the recorded cell is measured with a custom-made miniature thermo-microprobe connected to a monitoring thermometer (Model TH-8, Physitemp, Clifton, N.J.), and sampled using Digidata 1322A and pClamp 9.0 (Molecular Devices), as are the currents concurrently measured in the whole-cell patch clamp mode. The current is continuously sampled (at 100 Hz) at a holding potential of −60 mV.

Compounds of the formula (I) are diluted from 10 mM DMSO stocks (stored at −20° C.) into an extracellular solution either containing 100 μM menthol or subjected to cooling. Increasing concentrations of a compound are applied to a cell in a cumulative manner and concentration-dependent responses are measured after steady-state activation is achieved by either 100 μM menthol or cooling to 10° C. A saturating concentration of a reference antagonist is applied at the end of an experiment (either in the presence of 100 μM menthol or 10° C. temperature) to establish the baseline from which all the other measurements are subtracted.

Percentage inhibition by a compound is calculated as follows: 100×(1−I_(comp)/I₀); where I_(comp) and I₀ are steady-state current amplitudes in either the presence or absence of a concentration of compounds of the formula (I). Concentration-response data are fitted to a logistic function as follows: R=100/(1+c/IC₅₀)^(p); where, R is the percentage inhibition, p is the Hill coefficient and c is the concentration of compounds of the formula (I). Results are shown in Table 4.

TABLE 4 Mode of Cpd stimulation [μM] % inh n IC₅₀ (nM) 284 Cold 0.003 24.0 2 8.0 0.01 71.0 3 306 menthol 0.0003 11.6 3 1.1 0.001 47.3 3 0.003 78.0 3 0.01 94.9 3 306 cold 0.001 22.4 3 2.3 0.003 60.1 3 0.01 86.2 3 0.03 97.3 3 496 menthol 0.0001 27.5 3 0.183 0.0003 68.6 3 0.001 95.8 3 0.003 99.6 3 496 cold 0.0003 21.6 3 0.554 0.001 77.7 3 0.003 96.4 3

In Vivo Models Example 3 Inhibition of Icilin-Induced Behaviors in Rodents

Icilin was initially developed as a “super-cooling” compound by Delmar Chemicals Ltd. Subsequently it was shown to be one of the most potent known agonists of TRPM8 (McKerny D D, et al. Nature 2002, 416(6876): 52-8), having an EC₅₀=0.2 μM in stimulating calcium ion influx into TRPM8 transfected cells (Behrendt H J et al. Brit J Pharmacol 2004, 141(4): 737-45). Initial in vivo testing of icilin showed it to cause “wet-dog” shakes in rats. Similar shaking or jumping behavior was also evident in mice, rabbits, cats, dogs and monkeys. In humans, icilin produced a sensation of coolness on contact with mucous membranes, cold prickling when 0.1 mg was dropped on the tongue and coldness in the mouth, pharynx and chest lasting 30-60 minutes when 5-10 mg was ingested orally (Wei E T, Seid D A, J Pharm Pharmacol. 1983, 35, 110). The inhibition or reversal of icilin-induced shaking behaviors in rodents provides evidence for the utility of TRPM8 antagonists of the formula (I) in treating or preventing a disease, syndrome, disorder, or condition in a subject in which the disease, syndrome, disorder or condition is affected by the modulation of TRPM8 receptors.

Example 3a Inhibition of Icilin-Induced “Wet-Dog” Shakes in Rats

Male Sprague Dawley rats (220-450 g, Charles River Labs, n=6-9/treatment) were used to evaluate the ability of selected compounds of the formula (I) to block icilin-induced “wet-dog” shakes (WDS). Compounds of the formula (I) were administered in an appropriate vehicle, such as hydroxypropyl-β-cyclodextrin (HPβCD), methocellulose, 10% Solutol, or H₂O, or the like, by the appropriate route, i.p. or p.o., 30-120 minutes before icilin. Icilin was administered in PEG-400 or 10% solutol/H₂O, at 1.0 or 3.0 mg/kg, i.p. and spontaneous “wet-dog” shakes were counted 10-20 minutes post-icilin. Results are presented as a percent inhibition of shakes, which was calculated as [1−(test compound WDS count/vehicle WDS count)]×100. Results are shown in Table 5.

TABLE 5 Cpd Form Dose Route Vehicle Preicilin min % Inhibition ED50, mg/kg 271 CO₂ ⁻Na⁺ 30 p.o. Water 30 65 271 CO₂ ⁻Na⁺ 1 p.o. Water 30 28 5.7 3 35 10 46 30 88 272 CO₂ ⁻H 3 p.o. methocel 30 26 10 23 30 43 272 CO₂ ⁻H 30 p.o. HPbCD 30 37 272 CO₂ ⁻Na⁺ 10 p.o. HPbCD 30 0 30 72 272 CO₂ ⁻Na⁺ 3 p.o. HPbCD 30 0 22 10 29 30 74 100 75 273 CO₂ ⁻Na⁺ 30 p.o. HPbCD 30 39 273 CO₂ ⁻Na⁺ 10 p.o. HPbCD 30 17 53 30 25 100 71 283 CO₂ ⁻Na⁺ 30 p.o. HPbCD 30 65 283 CO₂ ⁻Na⁺ 3 p.o. HPbCD 30 13 10 −19 30 13 100 43 283 CO₂ ⁻Na⁺ 30 p.o. Water 30 71 296 CO₂ ⁻Na⁺ 30 p.o. HPbCD 30 27 306 CO₂ ⁻Na⁺ 30 p.o. HPbCD 60 99 306 CO₂ ⁻Na⁺ 3 p.o. HPbCD 60 63 10 99 30 100 306 CO₂ ⁻Na⁺ 0.3 p.o. HPbCD 60 39 2.5 1 9 3 64 10 98 306 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 99 307 CO₂H 30 p.o. HPbCD 30 13 309 CO₂H 30 p.o. HPbCD 30 23 361 CO₂H 30 p.o. HPbCD 30 87 361 CO₂ ⁻Na⁺ 3 p.o. Water 120 38 4.5 10 74 30 98 394 CO₂ ⁻Na⁺ 30 p.o. HPbCD 30 63 395 CO₂ ⁻Na⁺ 30 p.o. HPbCD 30 100 395 CO₂ ⁻Na⁺ 1 p.o. Water 60 15 7.6 3 26 10 55 30 88 396 CO₂ ⁻Na⁺ 30 p.o. HPbCD 30 99 398 CO₂ ⁻Na⁺ 30 p.o. HPbCD 30 7 400 CO₂ ⁻Na⁺ 30 p.o. HPbCD 30 84 409 CO₂ ⁻Na⁺ 30 p.o. HPbCD 30 16 427 CO₂ ⁻Na⁺ 30 p.o. Water 30 82 429 1H, Na tetrazole 30 p.o. HPbCD 30 41 429 1H, Na tetrazole 30 p.o. HPbCD 60 36 435 CO₂ ⁻Na⁺ 30 p.o. Water 30 41 479 CO₂ ⁻Na⁺ 30 p.o. HPbCD 60 77 480 CO₂ ⁻Na⁺ 30 p.o. HPbCD 60 39 483 1H, Na oxadiazole 30 p.o. Water w/NaOH 30 19 486 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 18 487 CO₂ ⁻Na⁺ 30 p.o. HPbCD 60 99 488 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 73 489 CO₂ ⁻Na⁺ 30 p.o. Water 60 99 490 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 84 496 CO₂ ⁻Na⁺ 30 p.o. Water 60 99 496 CO₂ ⁻Na⁺ 1 p.o. HPbCD 120 74 3 100 10 99 17.8 100 496 CO₂ ⁻Na⁺ 0.1 p.o. HPbCD 120 43 2.5 0.3 34 1 79 3 98 497 CO₂ ⁻Na⁺ 30 p.o. Water 60 96 502 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 14 505 CO₂ ⁻Na⁺ 30 p.o. HPbCD 60 72 519 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 −6 524 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 82 537 CO₂ ⁻Na⁺ 30 p.o. HPbCD 60 42 567 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 55 623 C(O)NNaSO₂CH₃ 10 p.o. HPbCD 60 38 627 1H, Na oxadiazole 30 p.o. HPbCD 60 0 635 1H, Na tetrazole 3 p.o. HPbCD 60 31 10 −8 30 53 56 72 640 1H, Na oxothiadiazole 30 p.o. HPbCD 60 20 657 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 32 658 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 63 755 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 99 756 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 100 784 1H, Na oxothiadiazole 30 p.o. HPbCD 60 79

Example 3b Reversal of Icilin-Induced Behaviors in Rats

Male Sprague Dawley rats (225-450 g, Charles River Labs, n=4-6/treatment) were used to evaluate the ability of selected compounds of the formula (I) to reverse icilin-induced “wet-dog” shakes. Icilin was administered in PEG-400 or 10% solutol/H₂O, at 1.0 or 3.0 mg/kg, i.p. and spontaneous “wet-dog” shakes (WDS) were counted 10-20 minutes post-icilin. Animals that exhibited 10 or more shakes were randomized into treatment groups and immediately administered compounds of the formula (I) in an appropriate vehicle, such as hydroxypropyl-β-cyclodextrin (HP β CD), methocellulose, 10% Solutol, or H₂O, or the like, and by the appropriate route, such as i.p. or p.o. Spontaneous “wet-dog” shakes were counted 60-70 minutes after compound administration. Results are presented as a percent inhibition of shakes, which was calculated as [1−(test compound WDS count/vehicle WDS count)]×100. Results are shown in Table 6.

TABLE 6 Cpd No. Dose (mg/kg) Route Post-icilin % Inhibition 2 30 p.o. 1 h 18 7 30 p.o. 1 h 65 13 30 p.o. 1 h 28 14 30 p.o. 1 h −16 15 30 p.o. 1 h −18 125 30 p.o. 1 h 39 148 30 p.o. 1 h 33 149 30 p.o. 1 h −3 168 30 p.o. 1 h −29 174 30 p.o. 1 h 45 177 30 p.o. 1 h 66 3 p.o. 1 h 15 10 p.o. 1 h 53 16.6 p.o. 1 h 54 30 p.o. 1 h 52 100 p.o. 1 h 52 188 30 p.o. 1 h 7

Example 3c Rightward Shift of Icilin Dose Effect Curve in Rats

Male Sprague Dawley rats (200-400 g, Charles River Labs, n=6-9/treatment) were administered icilin in a suitable vehicle (e.g. PEG-400, 10% Solutol) at 0.1-30 mg/kg, i.p. Spontaneous “wet-dog” shakes were counted 10-20 minutes post-icilin in order to generate a icilin dose-effect curve. A compound of the present invention was administered orally in hydroxypropyl-β-cyclodextrin 60 minutes before icilin challenge to assess the compound's ability to inhibit spontaneous “wet-dog” shakes (WDS) produced by a range of icilin doses. The ED50 of the icilin dose-effect curve generated in the presence of TRPM8 antagonist may be compared to that generated in the presence of vehicle to determine the magnitude of rightward shift as shown below in Table 7.

TABLE 7 Icilin ED50, Icilin ED50, mg/kg, i.p., mg/kg, i.p., Dose no compound Cpd (mg/kg) Route Pre-icilin pretreatment pretreatment 306 3 p.o. 60 0.75 2.96

Example 4 In Vivo Model of Subacute Inflammatory Pain: Carrageenan-Induced Hyperalgesia

Intraplantar injection of carrageenan into the hind paw of rats causes a robust acute inflammatory response characterized by reddening, swelling and hypersensitivity of the paw to thermal and mechanical stimuli typically peaking 3-6 hours following application and subsiding over the 12-24 hours.

Example 4a Rat Carrageenan-Induced Radiant Heat Hypersensitivity

To assess the effect of test compounds of the formula (I) on inflammatory hyperalgesia radiant heat response latencies were evaluated 3 hours following intraplantar carrageenan (Lambda, Type IV, 200 uL) injection into a single hind paw in male Sprague-Dawley rats. The test compound was administered either 2 hours prior to or 1 hour following carrageenan injection. The intent was to determine whether the compound would prevent or retard the hypersensitivity associated with this inflammogen. Baseline thermal response latencies were determined prior to any treatment and again 3 hours after carrageenan injection. Percent reversal of hyperalgesia relative to vehicle treatment (% R) was calculated for both compound treatment paradigms according to the following formula and is depicted in Table 8: % R=(Post compound latency−Post vehicle latency)/((Baseline latency−Post vehicle latency)×100%

TABLE 8 Percent Treatment Reversal, Cpd Time, hours relative to No. Salt Form Dose Route Vehicle relative to Cg vehicle 306 CO₂ ⁻Na⁺ 30 p.o. HPbCD −2 64 1 100 496 CO₂ ⁻Na⁺ 30 p.o. HPbCD −2 74 1 106

Example 5 In Vivo Model for of Chronic Inflammatory Pain: Complete Freund's Adjuvant (CFA)-Induced Hyperalgesia

Intraplantar injection of complete Freund's adjuvant (CFA) in rodents results in a long-lasting inflammatory reaction, characterized by a pronounced hypersensitivity to both thermal and mechanical stimuli. This hypersensitivity peaks between 24-72 hours following injection and can last for several weeks. To assess whether test compounds of the formula (I) reverse established hypersensitivity, a 100 μL intraplantar injection of CFA (suspended in a 1:1 emulsion of saline and heat-killed Mycobacterium tuberculosis in mineral oil) can be injected into a single hind paw of Sprague-Dawley rats (typically males ranging from 150-350 g). This paradigm also may be conducted with a multiple dosing or a prophylactic dosing regime designed to alter the course of hyperalgesia development. This test predicts the analgesic, anti-allodynic and antihyperalgesic effect of numerous effective clinical agents, including acetaminophen, NSAIDS such as aspirin and ibuprofen, and opioids, such as morphine.

Example 5a CFA-Induced Paw Radiant Heat Hypersensitivity

Each rat is placed in a test chamber on a warm glass surface and allowed to acclimate for approximately 10 minutes. A radiant thermal stimulus (beam of light) is then focused through the glass onto the plantar surface of each hind paw in turn. The thermal stimulus is automatically shut off by a photoelectric relay when the paw is moved or when the cut-off time is reached (20 seconds for radiant heat at ˜5 Amps). An initial (baseline) response latency to the thermal stimulus is recorded for each animal prior to the injection of CFA. Twenty-four hours following intraplantar CFA injection, the response latency of the animal to the thermal stimulus is then re-evaluated and compared to the animal's baseline response time. Only rats that exhibit at least a 25% reduction in response latency (i.e. hyperalgesia) are included in further analysis. Immediately following the post-CFA latency assessment, test compound or vehicle (usually Solutol, hydroxypropyl methylcellulose, hydroxypropyl beta-cyclodextrin or PEG-400) is administered i.p. or p.o. to rats. Post-compound treatment withdrawal latencies are assessed at fixed time intervals, typically 30, 60 and 120 minutes. The percent reversal (% R) of hypersenstivitiy is calculated according to the following formula: % Reversal=(Treatment Response−CFA Response)/(Baseline Response−CFA Response)×100.

TABLE 9 Cpd Salt High Treatment Percent No. Form Dose Route Vehicle Time, min Reversal ED50 306 CO₂ ⁻Na⁺ 10 p.o. HPbCD 100 91 306 CO₂ ⁻Na⁺ 3 p.o. HPbCD 100 31 4 5.6 76 10 93 30 59 361 CO₂ ⁻Na⁺ 10 p.o. HPbCD 100 28 496 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 79 496 CO₂ ⁻Na⁺ 1 p.o. HPbCD 60 9 3 −10 5.6 10 10 24 30 30 496 CO₂ ⁻Na⁺ 10 p.o. HPbCD 60 52

Example 5b CFA-Induced Paw Cold Hypersensitivity

Prior to intraplantar CFA injection, mice or rats are placed individually in elevated observation chambers having wire mesh floors. Through the mesh floor a series of three applications of acetone (0.04-0.10 mL/application) is sprayed onto the bottom of the paw using a multidose syringe device. A positive response takes the form of an abrupt withdrawal and licking of the paw. The cumulative duration of licking is recorded for each of the three trials which are then averaged to give the individual's response. Twenty-four hours following CFA injection acetone licking durations are markedly elevated implying a hypersensitivity to cooling. Test compounds of the formula (I) can be assessed for its ability to return acetone-evoked paw licking durations to pre-CFA levels (typically near zero) following systemic administration. Percent inhibition is calculated as follows % Inhibition=[1−(treatment licking duration/vehicle licking duration)]×100.

Example 6 Chemically-Induced Abdominal Irritant Models of Visceral Pain

A chemical irritant (such as acetic acid, kaolin, bradykinin, phenyl-p-(benzo) quinine, bromo-acetylcholine, or zymosan) is injected in mice intraperitoneally, causing a contraction of the abdominal musculature, which is characterized by an elongation of the body extending through to the hind limbs. The number of such responses is quantitated and is reduced by pretreatment of analgesic agents, thus forming the basis for a screening test (Collier H O et al. Br J Pharmacol Chemother 1968, 32(2): 295-310). This type of abdominal irritant test has been used to predict the analgesic effect of numerous clinically effective agents, the potency of which in the abdominal irritant test parallels the magnitude of the dose needed in the relief of clinical pain. Such agents include acetaminophen, NSAIDS such as aspirin and ibuprofen, opioids, such as morphine and codeine, and other centrally acting analgesics, such as tramadol.

One modification of the chemically-induced abdmonial irritant model of visceral pain is to pretreat animals with agents known to induce inflammatory responses following intraperitoneal injection (such as LPS, zymosan, or thioglycolate). A small intraperitoneal dose of such an inflammogen, administered hours or days before the acute chemical irritant challenge, has been shown to increase the number of abdominal contractions observed (Ribeiro R A, et al. Eur J Pharmacol 2000, 387(1): 111-8). While some analgesic agents are effective at mitigating acute viscerochemical nociception, others, particularly those dependent upon receptor induction are more effective at preventing or reversing the enhancement of behavioral responses caused by a preconditioning inflammatory stimulus. Because of the up-regulation of the TRPM8 receptor in inflammation, TRPM8 antagonists that are effective at reducing the mean number of contractions are predicted to provide analgesic action in human clinical use.

The ability of compounds of the formula (I) to mitigate chemical irritant-induced abdominal contractions following a pre-conditioning inflammatory stimulus can be studied as follows. Thioglycolate (3%, w/v, 2-3 mL i.p.) is injected into male CD1 mice (20-40 g, Charles River Labs), at a maximum dosage volume of 80 mL/kg, to induce peritoneal inflammation. Following a twenty-four hour pre-inflammation period these mice are dosed orally with compounds of the formula (I) (30 mg/kg; n=10) or vehicle (HPMC with 2% Tween80; n=9) and then one hour later subjected to an abdominal irritant challenge of acetic acid (1%, 10 mL/kg, i.p.). Immediately following injection of acetic acid, mice are placed individually in glass bell jars (approximately 15 cm in diameter) for counting of abdominal contractions over the next 15 minutes. The total number of abdominal contractions is summed for each treatment group and employed in the following formula to calculate Percent Inhibition (% I): % I=[1−(test compound contractions/vehicle contractions)]×100.

Example 7 In Vivo Models of Neuropathic Pain

The sciatic nerve is the major sensorimotor innervation of the (hind) leg and foot. Injury to the sciatic nerve or its constituent spinal nerves often results in pain-related behaviors. In rats and mice, tight ligation of the L5 spinal nerve with silk suture, partial tight ligation of the sciatic nerve with silk suture or loose ligation of the sciatic nerve with chromic gut suture each result in behaviors reminiscent of neuropathic pain in humans. These lesions (one per animal) are performed surgically in anesthetized rodents. Both the spinal nerve and sciatic nerve lesions result in allodynia, a painful response to normally innocuous stimuli, and hyperalgesia, an exaggerated response to normally noxious stimuli. It is important to note that both of these pain-related behaviors are evoked by the testing procedures and that normal use of the paw (e.g., walking) is relatively uncompromised, apart from occasional “guarding” of the paw. Subsequent to the surgery, the subjects' behaviors, such as grooming, feeding, and weight gain, are normal, except for hypersensitivity (as defined above) of the affected paw.

In addition to induction by nerve damage resulting from accidental trauma or surgical procedures, neuropathic pain can also be induced by diabetes (Fox, A et al., Pain 81:307-316, 1999) or by treatment with chemotherapeutic agents, such as paclitaxel or vincristine (Yaksh, T L et al., Pain 93:69-76, 2001).

Agents that attenuate neuropathic pain in the clinic also are effective in rodent neuropathic pain models. These agents include the recently approved Cymbalta (Duloxetine, Iyengar, S., et al., JPET 2004 311:576-584), morphine (Suzuki, R et al., Pain 1999 80:215-228) and gabapentin (Hunter, J C et al., Eur J Pharmacol 1997 324:153-160). The dual TRPV1/TRPM8 receptor antagonist BCTC reduced mechanical hyperalgesia and tactile allodynia in the chronic constriction injury rodent neuropathic pain model (Pomonis, J D et al., JPET 2003 306:387-393; Behrendt, H et al., Brit J Pharm 2004 141:737). Cold allodynia is a particularly debilitating symptom of neuropathic pain conditions (Jorum E et al. Pain 2003 101: 229-235). The antiallodynic effect of compounds of the formula (I) in this rodent model is predictive of clinical effect for these novel agents.

Example 7a Chronic Constriction Injury (CCI)-Induced Model of Neuropathic Pain-Acetone-Induced Hypersensitivity

Male Sprague Dawley rats (225-450 g; n=5-8/treatment) were used to evaluate the ability of selected compounds of the formula (I) to reverse CCI-induced cold hypersensitivity. Four loose ligatures of 4-0 chromic gut were surgically placed around the left sciatic nerve under inhalation anesthesia as described by Bennett et al (Bennett GJ, Xie Y K. Pain 1988, 33(1): 87-107). Fourteen to 35 days following CCI surgery, subjects were placed in elevated observation chambers containing wire mesh floors and five applications of acetone (0.05 mL/application separated by approximately 5 minutes) were spritzed onto the plantar surface of the paw using a multidose syringe. An abrupt withdrawal or lifting of the paw was considered a positive response. The number of positive responses was recorded for each rat over the five trials. Following baseline withdrawal determinations, compounds of formula (I) are administered in an appropriate vehicle, such as hydroxypropyl-β-cyclodextrin (HP β CD), methylcellulose, Methocel, 10% Solutol, or H₂O, or the like, by the appropriate route, i.p. or p.o. The number of withdrawals were redetermined 1 to 3 h after compound administration. Results are presented as a percent inhibition of shakes, which was calculated for each subject as [1-(test compound withdrawals/pre-test withdrawals)]×100 and then averaged by treatment. Results are shown in Table 10.

TABLE 10 Route of Pretreatment Percent Cpd No. Salt Form Dose, mg/kg Administration Vehicle Time, hr Inhibition ED50, mg/kg 7 CO₂H 30 p.o. 10% Solutol 1 47 30 i.p. 10% Solutol 2 66 177 CO₂H 3 p.o. 10% Solutol 1 23 10 49 30 46 100 70 30 i.p. 10% Solutol 3 60 292 CO₂ ⁻Na⁺ 30 p.o. Water 2 60 292 CO₂ ⁻Na⁺ 3 p.o. Water 3 7 70 10 16 30 21 100 67 272 CO₂ ⁻Na⁺ 30 p.o. HPbCD 1 31 273 CO₂ ⁻Na⁺ 30 p.o. HPbCD 0.5 49 271 CO₂ ⁻Na⁺ 30 p.o. HPbCD 1 77 271 CO₂ ⁻Na⁺ 10 p.o. HPbCD 1 24 30 44 100 56 306 CO₂ ⁻Na⁺ 30 p.o. HPbCD 6 69 306 CO₂ ⁻Na⁺ 3 p.o. HPbCD, Water 4 20 15 10 38 17.8 57 30 68 56 77 100 77 361 CO₂ ⁻Na⁺ 30 p.o. Water 4 74 361 CO₂ ⁻Na⁺ 3 p.o. Water 2 9 13 10 17 30 91 395 CO₂ ⁻Na⁺ 30 p.o. Water 2 23 395 CO₂ ⁻Na⁺ 30 p.o. Water 2 38 396 CO₂ ⁻Na⁺ 30 p.o. Water 4 50 400 CO₂ ⁻Na⁺ 30 p.o. Water 1 40 400 CO₂ ⁻Na⁺ 30 p.o. Water 3 25 487 CO₂ ⁻Na⁺ 30 p.o. HPbCD 3 66 487 CO₂ ⁻Na⁺ 10 p.o. HPbCD 3 43 488 CO₂ ⁻Na⁺ 30 p.o. HPbCD 2 43 489 CO₂ ⁻Na⁺ 30 p.o. Water 3 86 489 CO₂ ⁻Na⁺ 10 p.o. Water 4 13 23 17.8 60 30 57 56 70 490 CO₂ ⁻Na⁺ 30 p.o. HPbCD 1 23 496 CO₂ ⁻Na⁺ 30 p.o. Water 2 74 496 CO₂ ⁻Na⁺ 10 p.o. Water 4 76 17.8 64 30 72 56 68 496 CO₂ ⁻Na⁺ 0.3 p.o. HPbCD 4 28 3.5 1 32 3 23 5.6 72 10 71 497 CO₂ ⁻Na⁺ 30 p.o. Water 4 60 505 CO₂ ⁻Na⁺ 30 p.o. HPbCD 1 11 524 CO₂ ⁻Na⁺ 30 p.o. HPbCD 3 46

Example 7b

Chronic Constriction Injury (CCI)-Induced Model of Neuropathic Pain-Cold Plate-Induced Hypersensitivity

In male SD rats (175-325 g), four loose ligatures of 4-0 chromic gut are surgically placed around the left sciatic nerve under inhalation anesthesia as described by Bennet et al (Bennett G J, Xie Y K. Pain 1988, 33(1): 87-107). Seven to 21 days following sciatic chronic constriction injury (CCI) surgery, the subjects can be placed onto a commercial cold plate device cooled by peltier elements such that the surface temperature is held at 1° C. Each subject can undergo a 6 minute conditioning period followed by a 3 minute assessment period during which the total duration of hind paw lifting is recorded. This procedure is repeated at several intervals prior to and following systemic drug administration. Compounds of the formula (I) can be assessed for their ability to return duration of paw lifting back to pre-lesion levels. The duration of paw lifting during the 3 minute test period following administration of test compound is taken as a percentage of the duration of paw lifting during the 3 minute test period prior to test compound treatment.

Example 7c Chronic Constriction Injury (CCI)-Induced Model of Neuropathic Pain-Mechanical Allodynia (von Frey Test)

In male SD rats (175-325 g), four loose ligatures of 4-0 chromic gut are surgically placed around the left sciatic nerve under inhalation anesthesia as described by Bennet et al (Bennett G J, Xie Y K. Pain 1988, 33(1): 87-107). Seven to 21 days following sciatic chronic constriction injury (CCI) surgery, the subjects can be placed onto an elevated rack of plexigas chambers having wire mesh or another type of perforated flooring. The measurement of mechanical allodynia can be performed using the von Frey hairs (Semmes-Weinstein Monofilaments, Stoelting Co., IL) wherein the rats can be habituated to the wire mesh bottom cages before the start of the experiment. Static allodynia can be tested in the unrestrained rats by touching the plantar surface of the hind paw with von Frey hairs in ascending order of force (1.2, 1.5, 2.0, 3.6, 5.5, 8.5, 12, 15, 29, and 76 g) for up to 6 s or until a paw withdrawal response can be elicited. The lowest amount of force required to elicit a response can be recorded as the withdrawal threshold in log g. This procedure is repeated at several intervals prior to and following systemic drug administration. Compounds of the formula (I) can be assessed for their ability to return the threshold force which elicits paw lifting back to pre-lesion levels.

Example 8 Inflammatory Agent-Induced Models of Pyresis/Antipyresis

Compounds of the formula (I) can be tested in animal models of pyresis, according to previously documented and validated methods, such as those described by Kozak et al (Kozak W, Fraifeld V. Front Biosci 2004, 9: 3339-55). Fever is a frequent accompaniment of inflammatory disease. Animal models make use of the pyretic properties of yeast and other inflammatory agents, injecting a yeast suspension or other agent subcutaneously (Tomazetti J et al. J Neurosci Methods 2005, 147(1): 29-35); Van Miert A S, Van Duin C T. Eur J Pharmacol 1977, 44(3): 197-204). For example, Male Wistar rats (75-100 g) can be housed in groups of four to a cage at controlled temperature (23±1° C.) with a 12 h light:12 h dark cycle (lights on at 07:00 h) and with standard lab chow and tap water ad libitum. All measured temperatures can be taken between 08:00 and 19:00 h. Each animal can be used in only one study. Rectal temperature (TR) can be measured by inserting a lubricated thermistor probe (external diameter: 3 mm) 2.8 cm into the rectum of the animal. The probe can be linked to a digital device, which displayed the temperature at the tip of the probe with a 0.1° C. precision and logs the values over time. Immediately after measuring the initial basal rectal temperature, the animals can be injected with commercially available dried baker yeast (Saccharomyces cerevisiae) suspended in pyrogen-free 0.9% NaCl (0.05-0.25 g/kg, i.p.) or 0.9% NaCl (10 ml/kg). TR changes can be recorded every hour up to 12 h, and expressed as the difference from the basal value. Since it has been previously reported that handling and temperature measuring-related stress alter rectal temperature, these animals can be habituated to the injection and measuring procedure for 2 days before experiments are carried out. In these sessions, the animals can be subjected to the same temperature measuring procedure described above, and can be injected intraperitoneally (i.p.) with 0.9% NaCl (10 ml/kg).

To assess the effect of potential antipyretic compounds on basal rectal temperature study animals can have their TR measured for 4 h, and after the fourth TR measurement they can be subcutaneously (s.c.) injected with vehicle (such as 10% Solutol in sterile water 5 ml/kg) or compounds of the formula (I) prepared in vehicle. TR can then be recorded every hour up to 8 h after the compound injections. To assess the effect of compounds of the formula (I) on baker yeast-induced hyperthermia, study animals can have their basal TR measured and then be injected with a pyrogenic dose of baker yeast (for example, 0.135 g/kg). TR changes can be recorded every hour up to 4 h, when potential antipyretics agents such as those compounds of the formula (I) are administered. Rectal temperature can then be monitored over the following 8 h. Basal rectal temperature and changes in rectal temperature can be expressed as means±S.E.M. of the differences from TR at 07:00 h. Data can be analyzed by two-way analysis of variance (ANOVA), with time of measures treated as within subject factor, depending on the experimental design. Post hoc analysis can be carried out by the F-test for simple effect and the Student-Newman-Keuls test, when appropriate. A value of P<0.05 would be considered statistically significant.

The modification of the subsequent pyretic response by therapeutic agents can also be monitored by rectal telemetry or other measurements of body temperature. Several clinically relevant agents such as acetaminophen, aspirin and ibuprofen, reduce fever in these models. The antipyretic effect of TRPM8 antagonists, such as compounds of the formula (I), in these tests would also be predictive of their clinical effect.

Example 9 CFA-Induced Model of Rheumatoid Arthritis

Compounds of the formula (I) can be tested in animal models of rheumatoid arthritis, according to previously documented and validated methods, such as those described by Nagakura et al (Nagakura Y, et al. J Pharmacol Exp Ther 2003, 306(2): 490-7). For example, arthritis can be induced by the CFA inoculation in the rats (Male Lewis rats 150-225 g; Charles River). Briefly, 100 mg of Mycobacterium butyricum (Difco, Detroit, Mich.) can be thoroughly mixed with 20 mL of paraffin oil. Then mixture can be autoclaved for 20 min at 120° C. Each rat can be injected in the right footpad (hind paw) with the mixture in a 0.1-mL volume under inhalation anesthesia. The rats serving as controls can be injected with 0.1 mL of saline. Pain and other disease development parameters can be measured in the CFA- or saline-treated rats just before inoculation and up to 28 days post-inoculation. The measurement for pain parameters can be conducted for both mechanical and thermal (hot or cold) endpoints. The measurement of mechanical allodynia can be performed using the von Frey hairs (Semmes-Weinstein Monofilaments, Stoelting Co., IL) wherein the rats can be habituated to wire mesh bottom cages before the start of the experiment. Static allodynia can be tested in the unrestrained rats by touching the plantar surface of the hind paw with von Frey hairs in ascending order of force (1.2, 1.5, 2.0, 3.6, 5.5, 8.5, 12, 15, 29, and 76 g) for up to 6 s or until a paw withdrawal response can be elicited. The lowest amount of force required to elicit a response can be recorded as the withdrawal threshold in log g. Thermal hyperalgesia can be assessed using the radiant heat test wherein a mobile radiant heat source can be located under a glass surface upon which the rat is placed. The beam of light can be focused on the hind paw, and the paw withdrawal latencies are defined as the time taken by the rat to remove its hind paw from the heat source. The measurement of joint hyperalgesia can be performed by a modification of the previously reported method (Rupniak N M J et al. Pain 1997, 71: 89-97). The torso of each rat can be held from the back with the left palm, and the bending and extension (one after the other and five times in each direction) of the ankle within its limits of range of motion can be performed with the right fingers. The total number of vocalizations emitted after the manipulation (the bending and extension, five times in each direction) can be recorded for each paw (the maximum score is 10 for each paw).

The scoring of mobility can be performed by modifying the evaluation scale reported by Butler et al. (Butler S H et al Pain 1992, 48: 73-81): score 6, walks normally; score 5, walks being protective toward the ipsilateral hind paw (touches the ipsilateral hind paw fully on the floor); score 4, walks being protective toward the ipsilateral hind paw (touches only the toe of the ipsilateral hind paw on the floor); score 3, walks being protective toward both hind paws (touches the contralateral hind paw fully on the floor); score 2, walks being protective toward both hind paws (touches only the toe of the contralateral hind paw on the floor); score 1, crawls only using the fore paws; and score 0, does not move. Paw volumes can be measured by volume displacement of electrolyte solution in a commercially available plethysmometer device. The hind paw can be immersed to the junction of the hairy skin, and the volumes can be read on a digital display. The scoring of joint stiffness can be performed as follows: the body of rats can be held from the back with the left palm, and the bending and extension (once in each direction) of the ankle within its limits of range of motion can be performed with the right fingers. It can be confirmed beforehand that there is no restriction of ankle joint movement in the bending and extension manipulations in naive rats, and the scoring can be performed according to the evaluation scale reported by Butler (Butler S H et al Pain 1992, 48: 73-81): score 2, there are restrictions of full range of movement of the ankle in both bending and extension; score 1, there is a restriction of full range of movement of the ankle in bending or extension; and score 0, no restriction. The measurements for paw volume and joint stiffness can be conducted for both hind paws.

Compounds of the formula (I) can be assessed for antihyperalgesic efficacy as follows: thirty-two rats (8 rats per dose and four doses per compound) that are be treated with the CFA and another eight rats as naive controls can be used for each drug evaluation. The analgesic effects can be evaluated on post-inoculation day 9, when mechanical allodynia, thermal hyperalgesia, joint hyperalgesia, and joint stiffness in the ipsilateral paw reached almost the maximum, although those parameters in the contralateral paw changed only slightly and the systemic disturbance shown by the change of mobility score is small. On the day before evaluation, body weight, mechanical allodynia, thermal hyperalgesia, and joint hyperalgesia can be measured for the 32 rats that are to be used for compound evaluation. The rats are allocated to four groups (eight rats per group) such that the differences in the averages of those parameters among the groups became small. All the analgesic effect evaluations and behavioral observations can be carried out by the observer who is blind to the drug treatment.

Data can be expressed as the mean+/−S.E.M. The time-course curves for mechanical allodynia, thermal hyperalgesia, joint hyperalgesia, body weight, and paw volume can be subjected to two-way repeated measures analysis of variance with post hoc t test. In experiments for evaluation of compounds of formula (I), the difference in scores between the vehicle-treated and naive control groups can be analyzed by Student's t test to confirm significant changes in the pain parameters in the ipsilateral paw. The analgesic effects can be analyzed by Dunnett's t test, and in each case the drug-treated groups can be compared with the vehicle-treated group. In each statistical analysis, the comparison can be conducted for paws on the corresponding side. P<0.05 is considered statistically significant. In this model, the centrally acting analgesics morphine and tramadol fully relieved pain, whereas the NSAIDs, indomethacin and diclofenacare partially effective, evidencing the model's clinical predictability. The analgesic effect of compounds of the formula (I) in this test would predict their clinical usefulness in treating arthritis.

Example 10 In Vivo Model for Arthritis: Inflammogen-Induced Hyperalgesia of the Knee Joint

Compounds of the formula (I) can be tested in animal models of osteoarthritis, according to previously documented and validated methods, such as those described by Sluka et al (Sluka K A, Westlund K N. Pain 1993, 55(3): 367-77). For example, male Sprague-Dawley rats (Harlan, Indianapolis, Ind.) weighing 225 to 350 g can be briefly anesthetized with vaporized halothane and then injected with a mixture of 3% carrageenan and 3% kaolin (100 μL in 0.9% sterile saline) into the joint cavity of one knee. After the injection, the animals can be returned to their cages until the time of testing. For behavioral testing animals can be placed in individual clear plastic cages on top of an elevated wire mesh surface that restricted movement. The animals should be allowed to acclimate for approximately 1 hour before testing. Von Frey filaments, as described above, can then be used to test for enhanced responses to mechanical stimuli. The filaments can be successively applied through the wire mesh perpendicularly to the plantar surface in between the pads of the third and fourth phalanges. The response threshold to mechanical stimuli can be determined before inflammation of the knee joint; 4 hours after inflammation to confirm the development of hyperalgesia; immediately after the administration of test compound such as those of Formula (I) i.e. 5 hours after inflammation; and at 8, 12, and 24 hours after inflammation.

The Kruskal-Wallis test, a nonparametric test, can be used to analyze the effects for frequency, intensity, and group for response to mechanical stimuli at baseline, 4 hours after inflammation, and after compound treatment (5 hours, 8 hours, 12 hours, and 24 hours after inflammation). Further post hoc testing between groups can be executed by using the Mann-Whitney signed rank test. The data can be presented as median with 25th and 75th percentiles. Significance is P≦0.05.

Additionally, the gait of the animal or other pain-related behavior can be scored as the dependent measure of the painful effect of the arthritis on the animal's activity (Hallas B, Lehman S, Bosak A, et al. J Am Osteopath Assoc 1997, 97(4): 207-14). The effect of test drug on the animal's normal behavior can be quantified from zero, meaning no response, to three for incapacitating impairment. Effective analgesic treatment includes the clinically used indomethacin (Motta A F, et al. Life Sci 2003, 73(15): 1995-2004). Thus the benefit of compounds of the formula (I) in this model would predict their clinical relevance.

Example 11 Sarcoma Cell-Induced Models of Bone Cancer Pain

Compounds of the formula (I) can be tested in animal models of bone cancer pain, according to previously documented and validated methods, such as those described in the scientific literature (E1 Mouedden M, Meert T F. Pharmacol Biochem Behav 2005, 82(1): 109-19; Ghilardi J R, et al. J Neurosci 2005, 25(12): 3126-31). In preparation for cell inoculation and tumor induction, osteolytic murine sarcoma cells (NCTC 2472, American Type Culture Collection (ATCC), Rockville, Md., USA) can be cultured in NCTC 135 medium (Invitrogen) containing 10% horse serum (Gibco) and passaged 2 times weekly according to ATCC guidelines. For their administration, cells can be detached by scraping and then centrifuged at 1000×g. The pellet can be suspended in fresh NCTC 135 medium (2.5×10⁶ cells/20 μL) and then used for intramedullary femur inoculation. Male C3H/HeNCr1 mice (25-30 g, Charles River Labs) can be used in such experiments. After induction of general anesthesia with xylazine (10 mg/kg i.p.) and ketamine (100 mg/kg i.p.) the left hind paw can be shaved and disinfected with povidone-iodine followed by 70% ethanol. A superficial incision of 1 cm can then be made over the knee overlaying the patella. The patellar ligament can then be cut, exposing the condyles of the distal femur. A 23-gauge needle can be inserted at the level of the intercondylar notch and the intramedullary canal of the femur to create a cavity for injection of the cells. Twenty microliters of media (sham animals) or media containing tumor cells (approximately 2.5×10⁶ cells) can then be injected into the bone cavity using a syringe. To prevent leakage of cells outside the bone, the injection site can be sealed with dental acrylic and the wound closed with skin stitches.

Pain behaviors can be evaluated in separate groups (n=6) of sham and bone tumor mice with confirmed hyperalgesia as assessed by spontaneous lifting behavior. Animals can be behaviorally tested during a 3-week period prior to and after tumor inoculation. Body weight of the mice can be recorded throughout the experimental period to help monitor general health status. To measure the spontaneous lifting, the animals can be habituated in a transparent acrylic cylinder of 20 cm diameter put on an horizontal surface and thereafter observed during 4 min for spontaneous lifting behavior of the left hind paw. After spontaneous lifting behavior assessment, animals can be immediately placed on a mouse rotarod (e.g. ENV-575M\, Med Associates Inc., GA, USA) at a speed of 16 rpm for 2 min wherein limb-use during forced ambulation is scored: 4=normal; 3=limping; 2=partial non-use of left hind paw; 1=substantial non-use of left hind paw; 0=non-use of left hind paw. Assessment of cold allodynia may be made by exposing the ipsilateral hind paw of the mouse to 5 repeated applications of acetone (20 μL) and quantifying the lift/licking frequency and/or duration. Post-mortem evaluation of bone destruction can be assessed by ACT processing followed by scanning using a system such as the Skyscan 1076 microtomograph system for small animal imaging (Skyscan 1076\, Skyscan, Aartselaar, Belgium). Measured histomorphometry parameters of bone destruction can be subsequently correlated with behavioral endpoints.

The antihyperalgesic, antiallodynic and disease modifying effects of compounds of the formula (I) can be tested in this murine model of bone cancer pain in separate groups (n=6 per dose group). Animals with confirmed hyperalgesia, as assessed by spontaneous or acetone-evoked lifting, can be behaviorally tested, for example, on days 15 and 22 after distal femur tumor inoculation before and 1 h after systemic administration of vehicle (e.g. 20% HPbCD in sterile water) or compounds of the formula (I). The statistical analysis can be performed by one-way ANOVA to compare behavioral measurements and bone parameters among the experimental groups. To compare behavioral measurements and bone parameters between sham and tumor-bearing animals, a Mann-Whitney U test can be used. Results are considered statistically significant at P<0.05 (two-tailed). Data are expressed as mean+/−S.E.M.

Bone cancer causes intense pain in humans, mimicked in animal models of bone cancer pain in rodents such as that described above. Analgesic treatments that are effective in this model include COX-2 inhibitors (Sabino M A, Ghilardi J R, Jongen J L, et al. Cancer Res 2002, 62(24): 7343-9) and high doses of morphine (Luger N M et al. Pain 2002, 99(3): 397-406), agents used clinically for pain relief in patients experiencing bone cancer pain. Because this model so closely mimics the human disease state, the finding that cold allodynia is a prominent symptom (Lee, Seong et al. Yonsei Med J 2005, 46(2): 252-9) strongly supports the concept that TRPM8 antagonists of the present invention will provide relief of pain associated with human bone cancer.

Example 12 Respiratory Irritant-Induced Models of Cough

Compounds of the formula (I) can be tested in animal models of antitussive activity, according to previously documented and validated methods, such as those described by: Tanaka, M. and Maruyama, K. J. Pharmacol. Sci 2005, 99(1), 77-82; Trevisani, M. et al., Throax 2004, 59(9), 769-72; and Hall, E. et al., J. Med. Microbiol. 1999, 48: 95-98. Testing is conducted in transparent ventilated chambers with a constant airflow of 400 mL/min. The tussive agent (citric acid 0.25 M or capsaicin 30 mM) can be nebulised via a miniultrasonic nebuliser with an output of 0.4 mL/min. The appearance of cough can be detected by means of a tie clip microphone and confirmed by the characteristic posture of the animal. The cough sounds can be recorded and digitally stored. A blinded observer subsequently counts the number of elicited cough efforts. In some cases, animals can be sensitized by pre-exposure to certain agents such as ovalbumin. A test compound can be administered to at the peak of irritant-induced cough to evaluate the antitussive effects of the compound. In addition, prophylactic or multiple dosing regimes can be utilized to evaluate the test compound for modulation of the onset and duration of irritant-induced cough. Variations of these tests predict the antitussive effects of effective clinical agents, including NMDA antagonists such as dextrorphan and dextromethorphan, opioids such as codeine, beta 2 agonists such as salbutamol and antimuscarinics such as ipratropium (Bolser, D. C. et al., Eur J Pharmacol 1995, 277(2-3), 159-64; Braga, P. C. Drugs Exper Clin Res 1994, 20, 199-203). The antitussive action of menthol in both guinea pig and humans Eccles R. Curr Allergy Asthma Rep 2003, 3(3): 210-4; Laude E A, et al. Pulm Pharmacol 1994, 7(3): 179-84; Morice A H, et al. Thorax 1994, 49(10): 1024-6) is predictive of the clinical utility of compounds of the formula (I) as antitussive agents.

Example 13 Chemical Irritant-Induced Models of Itch, Contact Dermatitis, Eczema and Other Manifestations of Dermal Allergy, Hypersensitivity and/or Inflammation

Compounds of the formula (I) can be tested in animal models of contact dermatitis or itch, according to previously documented and validated methods, such as those described in the scientific literature (Saint-Mezard P et al. Eur J Dermatol 2004, 14(5): 284-95; Thomsen J. S., et al. J Exp Dermatol 2002, 11(4): 370-5; Weisshaar E, et al. Arch Dermatol Res 1998, 290(6): 306-11; Wille J J, et al. Skin Pharmacol Appl Skin Physiol 1999, 12(1-2): 18-27). Mice (or species such as guinea pig or rat) can be sensitized with 25 mL of 0.5% dinitrofluorobenzene solution (DNFB diluted 4:1 in acetone:olive oil immediately before application or other haptens, such as 12-myristate-13 acetate, picryl chloride, oxazolone, capsaicin, arachidonic acid, lactic acid, trans-retinoic acid or sodium lauryl sulfate) painted to the shaved dorsal skin or untreated (controls). Five days later, 10 mL of 0.2% DNFB a nonirritant dose) can be applied onto both sides of the right ear and the same amount of solvent alone onto the left ear. Ear thickness can be monitored daily using a caliper. Compounds of the formula (I) can be administered at the peak of inflammation to evaluate the anti-allergy activity of compounds. In addition, prophylactic or multiple dosing regimes can be utilized to evaluate the test compound for modulation of the onset and duration of anti-allergy activity. Variations of these tests can predict the anti-allergy and itch activity of effective clinical agents. The ability of these models to predict the therapeutic effect of compounds in human dermal conditions is supported by the cross-species ability of serotonin to induce itch (Weisshaar E, Gollnick H. Skin Therapy Lett 2000, 5(5): 1-2, 5). Additionally, the contact sensitizing property of commercially important drugs and the ability of ion channel modulators to prevent and treat skin sensitization in these models (Kydonieus A, et al., Proceedings of the International Symposium on Controlled Release of Bioactive Materials 24th:23-24, 1997) demonstrate the therapeutic utility of compounds of the formula (I) in dermal sensitization.

Example 14 Chemical Irritant-Induced Models of Rhinitis and Other Manifestations of Nasal Hypersensitivity and/or Inflammation

Compounds of the formula (I) can be tested in animal models of rhinitis, according to previously documented and validated methods, such as those described in the scientific literature (Hirayama Y, et al. Eur J Pharmacol 2003, 467(1-3): 197-203; Magyar T, et al Vaccine 2002, 20(13-14): 1797-802; Tiniakov R L, et al. J Appl Physiol 2003, 94(5): 1821-8). Testing can be conducted in mouse, guinea pig, dog or human in response to intranasal challenge with one or more irritants such as cold air, capsaicin, bradykinin, histamine, pollens, dextran sulfate, 2,4-tolylene diisocyanate, Bordetella bronchiseptica, Pasteurella multodica or acetic acid. In some cases, animals can be sensitized by pre-exposure to certain agents including, but not limited to, ragweed or ovalbumin. Prior to or following irritant administration, the test subject can receive, respectively, the prophylactic or therapeutic administration one or more times of compounds of the formula (I), or vehicle control, by the enteral or parenteral route. Significant differences indicative of nasal rhinitis or sensitization for the test compound-treated subjects compared with vehicle-treated subjects can be taken as evidence of anti-rhinitis activity. Independent variables include dose, frequency and route of administration, time interval between prophylactic or therapeutic test compound administration and irritant challenge as well as sex and non-sex genotype of the test subject. The intimate role of neurogenic inflammation in these hypersensitivity states demonstrates that compounds of the formula (I) desensitize or block the sensitization underlying these disease states.

Example 15 Conflict-Induced Models of Anxiety, Panic Disorder and Other Non-Adaptive Stressful or Phobic Responses

Compounds of the formula (I) can be tested in animal models of anxiety, panic disorders and other non-adaptive responses, according to previously documented and validated methods, such as those described by Cryan and Holmes (Cryan J F, Holmes A. Nat Rev Drug Discov 2005, 4(9): 775-90) or Braw et. al. (Y. Braw et al. Behav Brain Res 2006, 167: 261-269). Specifically, for studies in rats, the following apparati may be utilized: an open-field arena (62 cm×62 cm) enclosed by opaque walls (30 cm high) and plus-maze consists of two open arms, 50 cm×10 cm, and two enclosed arms, 50 cm×10 cm×40 cm with an open roof, arranged such that the two arms of each type are opposite each other. The maze is elevated to a height of 70 cm. The walls of the enclosed arms are made from black Plexiglas, while the floors from white Plexiglas. Videotape recordings can be analyzed using the ‘Observer’ system (Noldus Information Technology). A subject rat can be removed from its home cage, weighed and placed gently in the center of the open-field arena. The rat can be allowed to explore the open-field freely while its behavior is videotaped for 5 min. Afterwards, it can be transferred to the plus-maze and placed at the center, facing a closed arm. The rat's behavior can again be videotaped for 5 min, after which it can be returned to its home cage. The apparatus can cleaned using a 70% ethanol solution between rats.

Open-field and plus-maze measures can be grouped into two behavioral classes, namely ‘anxiety-like behaviors’ and ‘activity’. Open-field behavioral measures may include 1) Anxiety measures: % time in center square, % number of entries to center square (from total squares entered), % time freezing, latency to first freezing (freezing is scored when the subject is in an immobile state for at least 3 seconds; and 2) Activity measures: Total squares entered, number of rearings (standing on two hind legs), latency for first rearing. Plus-maze measures may include 1) Anxiety: % time in open arms, % number of entries to open arms (from total entries), number of unprotected head dips, latency to enter open arm; and 2) Activity: Total entries to all arms. Anxiety-like behaviors and activity can be analyzed by one-way ANOVA's on each of the measures, for each the between-subject comparisons. Plus-maze analyses can be conducted in a similar fashion.

Testing may also be conducted in mouse or rat in this fashion in order to measure avoidance of other aversive environmental stimuli such as Geller or Vogel anticonflict tests, the light/dark test and the hole-board test (see Cryan J F, Holmes A. Nat Rev Drug Discov 2005, 4(9): 775-90). Prior to environmental exposure, the test subject can receive the prophylactic administration one or more times of compounds of the formula (I), or vehicle control (e.g. 10% Solutol in sterile water), by the enteral or parenteral route. The cumulative time or number of times spent engaged in the aversive behavior can be measured. Significant differences in one or more of these measures for the test compound-treated subjects compared with vehicle-treated subjects can be taken as evidence of anxiolytic activity. Because these models are pharmacologically validated by the effectiveness of clinically useful anxiolytics (Cryan J F, Holmes A. Nat Rev Drug Discov 2005, 4(9): 775-90), they will be useful for the detection of anxiolytic compounds of the formula (I).

Example 16 Bladder Pressure- and Hypertrophy-Induced Models of Urinary Incontinence

Compounds of the formula (I) can be tested in animal models of urinary incontinence according to previously documented and validated methods, such as those described by in the scientific literature (Kaiser S, Plath T, (Metagen Pharmaceuticals GmbH, Germany DE Patent 10215321; McMurray G, et al. Br J Pharmacol 2006, 147 Suppl 2: S62-79). TRPM8 is expressed in human prostate, testicle, seminiferous tubules, scrotal skin and inflamed bladder (Stein R J, et al. J Urol 2004, 172(3): 1175-8; Stein R J, et al. J Urol 2004, 172(3): 1175-8; Mukerji et al. BMC Urology 2006, 6:6). Excitation of TRPM8 receptors through cooling or application of menthol causes contraction in the bladder and a decrease in micturation threshold volume (Tsukimi Y, Mizuyachi K, et al. Urology 2005, 65(2): 406-10). To assess compounds of the formula (I) for potential urinary incontinence activity, Sprague-Dawley rats are surgically implanted with bladder catheters allowing for the delivery of fluid (typically saline) and the monitoring of pressure (using a pressure transducer). Cystometry recordings can be monitored with a polygraph to evaluate voiding interval, threshold pressure, bladder capacity, bladder compliance, and the number of spontaneous bladder contractions. For example, the bladder catheter can be connected to a Harvard infusion pump, and bladders perfused overnight with saline at 2 mL/h. The next morning the bladder catheter can be attached (using a “T” connector) to a Statham pressure transducer (Model P23 Db) and to a Harvard infusion pump. A plastic beaker attached to a force displacement transducer (Grass FTO3) can be placed under the rat's cage to collect and record urine volume. The cystometric evaluation of bladder function can be started by infusing saline (20 mL/h) and after the first micturition the infusion is maintained for 20 min. Two hours after the first cystometry period, the rats can be dosed orally with compounds of the formula (I) and a second cystometry is performed between 30 min and 4 h after administration of test compound. The appropriate vehicle (e.g. 10% Solutol in sterile water) can be similarly administered to groups of rats that served as controls and the cystometry can be performed at the same respective time points.

Compounds of the formula (I) can also be evaluated under conditions of bladder hypertrophy and instability. Under anesthesia, a silk ligature is tied around the proximal urethra of rodents producing a partial outlet obstruction and subsequent hypertrophied bladder development within 6-9 weeks (Woods M. et al., J Urology 2001, 166:1142-47). Cystometry recordings can then be evaluated as described above. Such preclinical procedures are sensitive to compounds having clinical utility for the treatment of urinary incontinence (Soulard C, et al. J Pharmacol Exp Ther 1992, 260(3): 1152-8), and the activity of compounds of the formula (I) in this model would be predictive of clinical utility.

Example 17 In Vivo Model for Cold-Enhanced Central Pain States

Injury to the brain or spinal cord, such as that caused by trauma, interrupted blood flow or neurodegenerative diseases, often precipitates a central pain condition. Examples of such injuries characterized, in part by, a hypersensitivity to cold stimuli include multiple sclerosis (Morin C, et al. Clin J Pain 2002, 18(3): 191-5; Svendsen K B, et al. Pain 2005, 114(3): 473-81), stroke or cerebral ischemia (Greenspan J D, et al. Pain. 2004, 109(3): 357-66) and spinal cord injury (Defrin R, Ohry A, Blumen N, Urca G. Pain 2001, 89(2-3): 253-63; Defrin R, et al. Brain 2002, 125(Pt 3): 501-10; Finnerup N B, et al. Anesthesiology 2005, 102(5): 1023-30). Each of these conditions may be readily modeled in animals for assessment of the ability of compounds of the formula (I) to mollify the hypersensitive state. For example, a spinal cord injury (SCI) can be performed in adult Sprague-Dawley rats having a body weight of 150-200 g at time of surgery (Erichsen et al. Pain 2005, 116: 347-358). The rats can be anaesthetized with chloral hydrate (300 mg/kg, i.p., Sigma, USA) and a catheter can be inserted into the jugular vein. A midline skin incision can then be made along the back to expose the T11-L2 vertebrae. The animals can be positioned beneath a tunable argon ion laser (Innova model 70, Coherent Laser Products Division, CA, USA) operating at a wavelength of 514 nm with an average power of 0.17 W. The laser light can be focused into a thin beam covering the single T13 vertebra, which can be irradiated for 10 min. Immediately before the irradiation, erythrosin B (Aldrich, 32.5 mg/kg dissolved in 0.9% saline) can be injected intravenously via the jugular catheter. Due to rapid metabolism of erythrosin B, the injection can be repeated after 5 min in order to maintain adequate blood concentrations. During irradiation, the body core temperature can be maintained at 37-38° C. by a heating pad. After irradiation the wound can be closed in layers and the skin sutured together.

SCI rats can be routinely tested for the presence of pain-like behaviors from 3-4 weeks after surgery. The fur of the animals can be shaved at least a day prior to examination of the cutaneous pain threshold to avoid sensitization of the skin receptors. During testing, the rats can be gently held in a standing position by the experimenter and the flank area and hindlimbs can be examined for hypersensitivity to sensory stimulation. On the day of drug testing, SCI rats can be administered drug according to the experimental schedule and the time course of pain-like behaviors can be measured. To test for the presence of cold allodynia, ethyl chloride or acetone can be sprayed onto the skin of the animals, often that which has been previously determined to be sensitive to mechanical stimulation by von Frey filament testing. The subsequent response to cold stimulation can be observed and classified according to the following scale: 0, no visible response; 1, localized response (skin twitch) without vocalization; 2, transient vocalization; 3, sustained vocalization. Kruskal Wallis ANOVA on ranks can be used to analyze the overall effects of non-parametric data obtained in response to cold stimulation following pretreatment with either compounds of the formula (I) or vehicle.

Example 18 In Vivo Model for Post-Anesthetic Shivering

Spontaneous post-anesthetic tremor that resembles shivering is common during recovery from anesthesia. Risks to postoperative patients include an increase in metabolic rate of up to 400%, hypoxemia, wound dehiscence, dental damage, and disruption of delicate surgical repairs. The etiology of spontaneous post-anesthetic tremor is most commonly attributed to normal thermoregulatory shivering in response to intraoperative hypothermia. In most operating and recovery rooms, shivering is controlled by the use of humidifiers, warming blankets, and inhalation of humidified heated oxygen. However, pharmacological control is an effective alternate treatment modality (Bhatnagar S, et al. Anaesth Intensive Care 2001, 29(2): 149-54; Tsai Y C, Chu K S. Anesth Analg 2001, 93(5): 1288-92). Compounds of the formula (I) may be assessed for their ability to mitigate post-ansethetic induced-shaking by using animal models such as that described by Nikki et al (Nikki P, Tammisto T. Acta Anaesthesiol Scand 1968, 12(3): 125-34) and Grahn (Grahn, D A, et al. J Applied Physiology 1996, 81: 2547-2554). For example, Wistar rats (males, weighing 250-450 g) may be surgically implanted with an EEG/EMG recording array to assess post anesthetic tremor activity. The EEG electrodes are located bilaterally 2 mm off midline and adjacent to bregma and lamda. Following a one-week recovery period, frontal-occipital EEG, raw EMG, and integrated EMG activities, as well as three temperatures (skin, rectal, and water blanket temperatures during anesthesia), and ambient temperature post-anesthesia can be monitored throughout the experiment using copper-constantin thermocouples. The EEG and EMG signals can be recorded on polygraph paper (5 mm/s, Grass model 7E polygraph) and, during recovery from anesthesia, the EEG is computer scored in 10 second epochs as either synchronized: high amplitude (0.100 μV), low frequency (1-4 Hz dominated) activity characteristic of slow-wave sleep (SWS-like) or desynchronized: low amplitude (75 μV), high frequency (5-15 Hz dominated), characteristic of waking and rapid-eye-movement sleep (W-like). The EMG activity can be quantified as the averaged summed voltage/time interval by processing the raw EMG signal through an integrator (Grass model 7P3, 0.5 s time constant). On the day of an experiment, the animal can be placed in a small acrylic box (15×15×15 cm) and exposed to a halothane vapor-air mixture (4% halothane). Immediately after the induction of anesthesia, the animal can be removed from the enclosure and subsequently anesthetized through a nose cone. Following cessation of anesthesia, two stages of recovery can be judged: emergence from anesthesia and restoration of behavioral activity (behavioral recovery). Emergence from anesthesia may be defined as an increase in tonic EMG activity and a change in the EEG from a SWS-like pattern to a W-like pattern. Behaviorally, recovery has occurred when the animal rises from a prone position and initiated coordinated movements. The time intervals from termination of anesthesia to emergence and behavioral recovery can be measured in all animals. Time interval data can be subjected to a repeated measure analysis of variance, and the Scheffe's method can be employed for testing differences between pairs of means.

Example 19 Cold-Evoked Cardiovascular Pressor Responses

Compounds of the formula (I) can be tested in animals and humans for their ability to mitigate cardiovascular pressor responses evoked by cold exposure. Seasonal environmental cooling is directly associated with elevated blood pressure and an increased incidence of coronary events in human populations worldwide (Barnett, A G et al. J Epidemiol Community Heath 2005, 59 551-557). Cold-evoked pulmonary hypertention and cold aggravation of chronic obstructive pulmonary disease are clinical indications succeptible to heightened cardiopulmonary sensitivity to cold (Marno P et al. Eur Respiratory Review 2006, 15 (101): 185; Acikel M et al Int J of Cardiol (2004) 97: 187-192). The clinical cold pressor test assesses changes in blood pressure (BP) and cold pain perception during a 2-3 minute immersion of one hand into ice water. This test may be utilized to characterize analgesic compounds (Koltzenberg M et al. Pain 2006, 126(1-3): 165-74) and to assess cold hypersensitivity (Desmeules J A et al. Arthritis Rheum 2003, 48(5): 1420-9). Compounds of the formula (I) can be studied in an anesthetized rat cold pressor paradigm to determine whether TRPM8 antagonism would interfere with the blood pressure pressor response to cold stimulation of the forepaws. Male Sprague-Dawley rats (300-450 g) anesthetized with sodium pentobarbital are instrumented with a jugular catheter and an indwelling carotid artery cannula connected to a pressure transducer. Vehicle (e.g. 20% HPbCD in sterile water) or test compound is infused (1 mL/kg) over one minute through the intravenous catheter. Ten minutes later both forelimbs are packed in crushed ice for 5 minutes. Alternatively, the test compound and vehicle treatments may be administered orally at an appropriated time prior to the surgical cannulations and cold challenge. Percent changes in mean arterial pressure in response to this cold stimulus are calculated for vehicle and test compound pretreatments. Percent inhibition attributed to treatment with test compound is then determined using the following formula: % Inhibition=[1−(cold evoked % change in BP post-test compound/cold evoked % change in BP post-vehicle)]×100. Results are shown in Table 11

TABLE 11 Treatment Percent Time, hours Inhibition, Cpd relative to Cold relative to No. Salt Form Dose Route Vehicle Challenge vehicle 306 CO₂ ⁻Na⁺ 1 p.o. HPbCD 1.5 16 3 41 10 62 30 75

Example 20 Cold-Induced Vasoconstriction: Ramifications for Tissue Perfusion

Damage may occur to a bodily tissue when blood flow is compromised or interrupted. Reasons for vascular compromise include peripheral vascular disease (Lamah M et al, European journal of vascular and endovascular surgery (1999), 18(1), 48-51), prior traumatic or frostbite injury, Raynaud's syndrome (Lutolf, O et al Microvascular research (1993), 46(3), 374-82), diabetic neuropathy (Forst T et al, Clinical science (London, England: 1979) (1998), 94(3), 255-61.), surgical intervention and autonomic dysregulation (Gherghel D et al, Investigative ophthalmology & visual science (2004), 45(10), 3546-54). In the case of marginal resting perfusion, vasoconstriction as enchanced by cool temperature may aggravate symptoms and potentiate tissue injury (Cankar K et al, The Journal of hand surgery (2000), 25(3), 552-8; Lutolf O et al Microvascular research (1993), 46(3), 374-82.). Several of these conditions may be readily modeled in animals to assess of the ability of TRPM8 antagonists such as compounds of the formula (I) to preserve tissue perfusion in the face of local cooling. For example, laser Doppler assessment of skin blood flow may be studied in the paws of anesthetized rats (Hord A H et al, Anesthesia and analgesia (1999), 88(1), 103-8), wherein the paw is subject to a series of decreasing temperatures steps as applied by physical contact with a Peltier cooling element under computer control. The laser Doppler measures skin perfusion in the face of cooling-induced vasoconstriction thereby generating a temperature×perfusion relationship. Systemic administration of a TRPM8 antagonist is anticipated to shift this curve toward preserving perfusion at reduced temperatures relative to vehicle pretreatment. This activity is envisioned to be therapeutic in protecting tissue from hypo-perfusion and ischemia thereby minimizing the associated symptoms (e.g. pain) and potential tissue damage.

While the foregoing specification teaches the principles of the present invention, with examples provided for the purpose of illustration, it will be understood that the practice of the invention encompasses all of the usual variations, adaptations and/or modifications as come within the scope of the following claims and their equivalents. 

We claim:
 1. A method for treating inflammatory hyperalgesia in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a compound selected from the group consisting of: N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide and N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-carboxy-benzenesulfonamide.
 2. The method of claim 1 wherein the inflammatory hyperalgesia is inflammatory somatic hyperalgesia or inflammatory visceral hyperalgesia.
 3. A method for treating inflammatory somatic hyperalgesia in which a hypersensitivity to thermal stimuli exists, comprising administering to the subject a therapeutically effective amount of a compound selected from the group consisting of: N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide and N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-carboxy-benzenesulfonamide.
 4. A method for treating inflammatory visceral hyperalgesia in which a enhanced visceral irritability exists, comprising administering to the subject a therapeutically effective amount of a compound selected from the group consisting of: N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-fluoro-3-trifluoromethyl-benzyl)-4-carboxy-benzenesulfonamide and N-(3-Methyl-benzo[b]thiophen-2-yl)-N-(4-trifluoromethoxy-benzyl)-4-carboxy-benzenesulfonamide.
 5. The method of claim 1 wherein the inflammatory hyperalgesia is due to inflammation, osteoarthritis, rheumatoid arthritis, back pain, joint pain, abdominal pain, musculoskeletal diseases, skin diseases, post operative pain, headaches, fibromyalgia, toothache, burn, sunburn, insect sting, neurogenic bladder, urinary incontinence, interstitial cystitis, urinary tract infection, cough, asthma, chronic obstructive pulmonary disease, rhinitis, contact dermatitis/hypersensitivity, itch, eczema, pharyngitis, enteritis, irritable bowel syndrome, Crohn's Disease, or ulcerative colitis. 